SE-ATLAS

Frontonasal dysplasia Achondrogenesis Short rib-polydactyly syndrome, Saldino-Noonan type Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome Heart-hand syndrome type 3 X-linked dominant intellectual disability-epilepsy syndrome Syndactyly type 5 Oculocerebrofacial syndrome, Kaufman type Schinzel-Giedion syndrome Spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Spondyloepimetaphyseal dysplasia, Isidor-Toutain type Osteosclerosis-developmental delay-craniosynostosis syndrome HSD10 disease, infantile type Brachydactyly-syndactyly, Zhao type Global developmental delay-osteopenia-ectodermal defect syndrome Orofaciodigital syndrome type 9 Spastic ataxia-corneal dystrophy syndrome Short rib-polydactyly syndrome, Verma-Naumoff type Semilobar holoprosencephaly Spondylometaphyseal dysplasia Schwartz-Jampel syndrome Autosomal dominant deafness-onychodystrophy syndrome Intellectual disability-spasticity-ectrodactyly syndrome Juvenile hyaline fibromatosis Czeizel-Losonci syndrome Familial hypocalciuric hypercalcemia type 2 Filippi syndrome Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome Moynahan syndrome Difference of sex development-intellectual disability syndrome 9q31.1q31.3 microdeletion syndrome Albright hereditary osteodystrophy Thanatophoric dysplasia type 2 Multiple non-ossifying fibromatosis ATR-X-related syndrome Holoprosencephaly-postaxial polydactyly syndrome Congenital vertical talus X-linked dominant chondrodysplasia punctata Unilateral focal polymicrogyria Spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome Fibular dimelia-diplopodia syndrome Ruvalcaba syndrome Monostotic fibrous dysplasia Oculofaciocardiodental syndrome Arthrogryposis-hyperkeratosis syndrome, lethal form Familial hypocalciuric hypercalcemia type 3 Cenani-Lenz syndrome DOORS syndrome Isolated split hand-split foot malformation Autosomal dominant Opitz G/BBB syndrome Adult hypophosphatasia Alopecia-intellectual disability syndrome Oculo-palato-cerebral syndrome Rare genetic disease EEC syndrome Otopalatodigital syndrome 14q24.1q24.3 microdeletion syndrome Osteopetrosis-hypogammaglobulinemia syndrome Pterygium colli-intellectual disability-digital anomalies syndrome Oculocerebrorenal syndrome of Lowe IVIC syndrome Shoulder and girdle defects-familial intellectual disability syndrome Dobrow syndrome Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome Proximal Xq28 duplication syndrome Intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome Autosomal recessive multiple pterygium syndrome Syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome Spondyloepiphyseal dysplasia, Kimberley type Spondyloepiphyseal dysplasia, Reardon type Pyruvate dehydrogenase E3-binding protein deficiency Rare bone disease Spondyloepimetaphyseal dysplasia, PAPSS2 type Acrocephalosyndactyly Syndromic neurometabolic disease with X-linked intellectual disability Absence deformity of leg-cataract syndrome Symbrachydactyly of hand and foot, bilateral Autosomal recessive spondylocostal dysostosis X-linked creatine transporter deficiency SRD5A3-CDG Mohr-Tranebjaerg syndrome Reunion Island Larsen-like syndrome Ulbright-Hodes syndrome Severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome X-linked intellectual disability due to GRIA3 mutations Hereditary cryohydrocytosis with reduced stomatin Ectodermal dysplasia-pili torti-cutaneous syndactyly syndrome Say-Barber-Miller syndrome Congenital radioulnar synostosis MEDNIK syndrome Non-syndromic craniosynostosis Glossopalatine ankylosis Say-Field-Coldwell syndrome Multiple pterygium syndrome Amish infantile epilepsy syndrome Isolated osteopoikilosis Radioulnar synostosis-developmental delay-hypotonia syndrome Chudley-Lowry-Hoar syndrome X-linked intellectual disability, Najm type SCARF syndrome Ciliopathies with major skeletal involvement Baller-Gerold syndrome Lethal occipital encephalocele-skeletal dysplasia syndrome Holmes-Gang syndrome Spondyloepiphyseal dysplasia tarda, Kohn type Upington disease Congenital muscular dystrophy, Fukuyama type Smith-Fineman-Myers syndrome Central polydactyly of toes Hydrocephalus with stenosis of the aqueduct of Sylvius Heart-hand syndrome Hajdu-Cheney syndrome Blepharophimosis-intellectual disability syndrome, Ohdo type Carpenter-Waziri syndrome Banki syndrome Multiple metaphyseal dysplasia COG1-CDG Ulnar-mammary syndrome Spondyloepiphyseal dysplasia, MacDermot type Acropectororenal dysplasia Developmental delay-facial dysmorphism syndrome due to MED13L deficiency Multiple epiphyseal dysplasia and pseudoachondroplasia Brain-lung-thyroid syndrome Dyskeratosis congenita Primary hypertrophic osteoarthropathy Mandibuloacral dysplasia Odontohypophosphatasia Pyknoachondrogenesis Okihiro syndrome VACTERL with hydrocephalus Renier-Gabreels-Jasper syndrome Short stature, Brussels type Leukocyte adhesion deficiency type II Hypocalcemic vitamin D-dependent rickets Mirror polydactyly-vertebral segmentation-limbs defects syndrome Hypocalcemic vitamin D-resistant rickets X-linked complex spastic paraplegia Achondrogenesis type 2 Cole-Carpenter syndrome Leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome Mandibulofacial dysostosis-microcephaly syndrome Facial dysmorphism-shawl scrotum-joint laxity syndrome Osteopenia-intellectual disability-sparse hair syndrome Achondrogenesis type 1B Van den Ende-Gupta syndrome Spondylodysplastic dysplasia X-linked complicated spastic paraplegia type 1 Non-syndromic syndactyly Thin ribs-tubular bones-dysmorphism syndrome Spondyloepimetaphyseal dysplasia, Bieganski type Bartsocas-Papas syndrome Marden-Walker syndrome Hyperostosis corticalis generalisata Leukocyte adhesion deficiency type III Pfeiffer-Palm-Teller syndrome Hypochondrogenesis Periventricular nodular heterotopia Freeman-Sheldon syndrome Shprintzen-Goldberg syndrome Schneckenbecken dysplasia X-linked Charcot-Marie-Tooth disease type 1 Acromesomelic dysplasia Van den Bosch syndrome Neonatal severe primary hyperparathyroidism Osteochondritis of tarsal/metatarsal bone Achondrogenesis type 1A Coxopodopatellar syndrome Dysosteosclerosis Odontochondrodysplasia Acromelic dysplasia SHOX-related short stature Myopathy-growth delay-intellectual disability-hypospadias syndrome Brachyolmia, Maroteaux type Congenital pseudoarthrosis of the femur Stickler syndrome Campomelic dysplasia and related disorders Intellectual disability-cataracts-kyphosis syndrome Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome X-linked Charcot-Marie-Tooth disease type 2 Patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome Distal arthrogryposis Spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome Acrofrontofacionasal dysostosis Multiple epiphyseal dysplasia due to collagen 9 anomaly Distal Xq28 microduplication syndrome Mesomelic and rhizo-mesomelic dysplasia Congenital cataracts-facial dysmorphism-neuropathy syndrome Trichorhinophalangeal syndrome Autosomal dominant brachyolmia Metaphyseal acroscyphodysplasia X-linked Charcot-Marie-Tooth disease type 4 Brachyolmia type 1, Toledo type Acrofacial dysostosis, Catania type Fryns syndrome Craniodigital-intellectual disability syndrome Multiple epiphyseal dysplasia type 4 Acromicric dysplasia Kenny-Caffey syndrome Radio-renal syndrome Neonatal osteosclerotic dysplasia Congenital vascular bone syndrome Spondyloepimetaphyseal dysplasia, aggrecan type Polymicrogyria with optic nerve hypoplasia Nestor-Guillermo progeria syndrome FGFR2-related bent bone dysplasia Ophthalmoplegia-intellectual disability-lingua scrotalis syndrome Sclerosteosis Congenital knee dislocation Dysostosis with brachydactyly Temple syndrome due to paternal 14q32.2 microdeletion Progressive non-infectious anterior vertebral fusion McDonough syndrome Absent radius-anogenital anomalies syndrome Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome Chondrodysplasia punctata McCune-Albright syndrome Primary bone dysplasia with increased bone density Cataract-intellectual disability-anal atresia-urinary defects syndrome TMEM165-CDG Multiple epiphyseal dysplasia type 1 AICA-ribosiduria Isolated complex I deficiency Teebi-Shaltout syndrome Primary bone dysplasia with defective bone mineralization Zechi-Ceide syndrome Microcephalic primordial dwarfism Frontofacionasal dysplasia Isolated oxycephaly Ramon syndrome Cataract-deafness-hypogonadism syndrome Galloway-Mowat syndrome HSD10 disease, neonatal type Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia Hypochondroplasia SLC35A2-CDG Osteogenesis imperfecta Shwachman-Diamond syndrome Dyssegmental dysplasia, Rolland-Desbuquois type Spondylometaphyseal dysplasia, Czarny-Ratajczak type Craniodiaphyseal dysplasia Craniofrontonasal dysplasia Ectrodactyly-polydactyly syndrome Hepatic fibrosis-renal cysts-intellectual disability syndrome Enlarged parietal foramina Xeroderma pigmentosum-Cockayne syndrome complex Primary bone dysplasia with multiple joint dislocations Primary non-essential cutis verticis gyrata Aortic arch anomaly-facial dysmorphism-intellectual disability syndrome Pyruvate dehydrogenase E1-alpha deficiency Cooks syndrome Intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome Blepharophimosis-intellectual disability syndrome Phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome Primary bone dysplasia with decreased bone density Primary osteolysis Multiple epiphyseal dysplasia, Beighton type RAPADILINO syndrome 1p21.3 microdeletion syndrome Craniofrontonasal dysplasia-Poland anomaly syndrome Extensor tendons of finger anomalies Oromandibular-limb hypogenesis syndrome Mixed sclerosing bone dystrophy with extra-skeletal manifestations Craniometaphyseal dysplasia OBSOLETE: Peripheral dysostosis Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type SLC39A13-related spondylodysplastic Ehlers-Danlos syndrome Spondylometaphyseal dysplasia, 'corner fracture' type MEND syndrome Autosomal recessive hypophosphatemic rickets Microphthalmia, Lenz type Orofaciodigital syndrome type 1 Cleidocranial dysplasia and isolated cranial ossification defect Lethal congenital contracture syndrome type 2 Cataract-intellectual disability-hypogonadism syndrome Orofaciodigital syndrome type 2 Primary bone dysplasia with disorganized development of skeletal components Microcephaly-brachydactyly-kyphoscoliosis syndrome Autosomal dominant spondylocostal dysostosis Megalocornea-intellectual disability syndrome Isolated cloverleaf skull syndrome Spondylometaphyseal dysplasia, Sedaghatian type MMEP syndrome Dominant hypophosphatemia with nephrolithiasis or osteoporosis Cranio-osteoarthropathy Acrocapitofemoral dysplasia Orofaciodigital syndrome type 4 Dysostosis with predominant vertebral and costal involvement X-linked calvarial hyperostosis Lethal congenital contracture syndrome type 3 Dysostosis with predominant craniofacial involvement Multiple epiphyseal dysplasia, Lowry type Isolated Klippel-Feil syndrome Temple syndrome due to maternal uniparental disomy of chromosome 14 Peters plus syndrome Craniosynostosis, Philadelphia type Melhem-Fahl syndrome Orofaciodigital syndrome type 8 Omphalocele syndrome, Shprintzen-Goldberg type Sagliker syndrome Angelman syndrome due to imprinting defect in 15q11-q13 Brachydactylous dwarfism, Mseleni type Tetraamelia-multiple malformations syndrome Autosomal recessive Stickler syndrome Orofaciodigital syndrome type 12 Patellar dysostosis Pfeiffer syndrome Orofaciodigital syndrome type 10 Alpha-thalassemia-X-linked intellectual disability syndrome Blepharophimosis-radioulnar synostosis syndrome Arthrogryposis syndrome Acrofacial dysostosis, Kennedy-Teebi type Dysostosis of genetic origin with limb anomaly as a major feature Radial hemimelia Syndromic X-linked intellectual disability 7 Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type Melnick-Needles syndrome Multicentric osteolysis-nodulosis-arthropathy spectrum Tibial hemimelia Kleefstra syndrome Non-syndromic polydactyly, syndactyly and/or hyperphalangy Biemond syndrome type 2 X-linked intellectual disability, Abidi type Cerebrofaciothoracic dysplasia Melorheostosis Bipartite talus Central polydactyly of toes, bilateral Shoulder and thorax deformity-congenital heart disease syndrome X-linked intellectual disability-epilepsy syndrome Non-syndromic limb reduction defect 17q11 microdeletion syndrome Familial clubfoot due to 17q23.1q23.2 microduplication Orofaciodigital syndrome type 13 Hypertelorism-microtia-facial clefting syndrome Fallot complex-intellectual disability-growth delay syndrome X-linked intellectual disability, Armfield type Pseudoaminopterin syndrome Ulnar hypoplasia-split foot syndrome Syndrome with limb malformations as a major feature Imperforate oropharynx-costovertebral anomalies syndrome Sillence syndrome Autosomal recessive Kenny-Caffey syndrome Gómez-López-Hernández syndrome Microphthalmia-ankyloblepharon-intellectual disability syndrome Caudal appendage-deafness syndrome Sirenomelia Fibular hemimelia Postaxial polydactyly of toes, unilateral Geroderma osteodysplastica Syndrome with synostosis or other joint formation defect Tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome Craniosynostosis-fibular aplasia syndrome Multiple pterygium-malignant hyperthermia syndrome Non-syndromic limb malformation KDM5C-related syndromic X-linked intellectual disability Bonnemann-Meinecke-Reich syndrome Delayed membranous cranial ossification Upper limb defect-eye and ear abnormalities syndrome Postaxial polydactyly of toes, bilateral Multiple epiphyseal dysplasia, Al-Gazali type Progressive osseous heteroplasia Autosomal dominant Kenny-Caffey syndrome Christianson syndrome Bilateral parasagittal parieto-occipital polymicrogyria 48,XYYY syndrome Brachyolmia-amelogenesis imperfecta syndrome Eyebrow duplication-syndactyly syndrome Rare surgical thoracic disease Agnathia-holoprosencephaly-situs inversus syndrome Osteocraniostenosis Dysostosis of genetic origin Autosomal dominant omodysplasia Rubinstein-Taybi syndrome due to EP300 haploinsufficiency Frontorhiny RFT1-CDG Leri pleonosteosis Central polydactyly of toes, unilateral Osteochondritis dissecans Tatton-Brown-Rahman syndrome Weaver syndrome Metaphyseal chondrodysplasia, Schmid type Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome Marfan syndrome type 1 Delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome X-linked intellectual disability, Miles-Carpenter type Osteosclerosis-ichthyosis-premature ovarian failure syndrome Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to WWOX deficiency Lethal chondrodysplasia Okihiro syndrome due to 20q13 microdeletion Cartilage-hair hypoplasia Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia Thalidomide embryopathy Carpotarsal osteochondromatosis MEHMO syndrome X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome X-linked intellectual disability, Schimke type Roifman syndrome Jackson-Weiss syndrome Mesomelic dwarfism-cleft palate-camptodactyly syndrome Intellectual disability-strabismus syndrome Weill-Marchesani syndrome Bilateral frontal polymicrogyria X-linked mandibulofacial dysostosis Synpolydactyly type 1 Weissenbacher-Zweymuller syndrome Craniosynostosis, Boston type Rhizomelic chondrodysplasia punctata type 1 Langer mesomelic dysplasia Intellectual disability-balding-patella luxation-acromicria syndrome Thiemann disease, familial form Non-syndromic sagittal craniosynostosis Familial osteodysplasia, Anderson type BRESEK syndrome Postaxial polydactyly type A Infantile spasms syndrome Multiple epiphyseal dysplasia, with miniepiphyses Upper limb mesomelic dysplasia Pelviscapular dysplasia X-linked intellectual disability, Shashi type Muscle-eye-brain disease Bowen-Conradi syndrome Epiphyseal stippling-osteoclastic hyperplasia syndrome Mesomelic dwarfism, Reinhardt-Pfeiffer type Genetic syndrome with limb reduction defects Treacher-Collins syndrome Bruck syndrome Spondylocamptodactyly syndrome Familial clubfoot due to 5q31 microdeletion Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome Chondroectodermal dysplasia with night blindness Polydactyly of a triphalangeal thumb X-linked intellectual disability, Vitale type Zygodactyly type 3 GMS syndrome Lacrimoauriculodentodigital syndrome Metachondromatosis Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency X-linked intellectual disability, Stocco Dos Santos type Intellectual disability-developmental delay-contractures syndrome Bilateral generalized polymicrogyria Crisponi syndrome Postaxial polydactyly type B Hyperekplexia-epilepsy syndrome FRAXE intellectual disability 20q11.2 microduplication syndrome Angelman syndrome due to maternal 15q11q13 deletion Polysyndactyly X-linked intellectual disability, Wittwer type Wiedemann-Rautenstrauch syndrome Isolated plagiocephaly FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome Polydactyly of a biphalangeal thumb and/or hallux Wildervanck syndrome 2q37 microdeletion syndrome Multicentric carpo-tarsal osteolysis with or without nephropathy Blepharophimosis-intellectual disability syndrome, SBBYS type Okihiro syndrome due to a point mutation Femoral agenesis/hypoplasia, unilateral Rhizomelic chondrodysplasia punctata type 2 Thrombocytopenia-absent radius syndrome Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome Poland syndrome Polydactyly of an index finger X-linked intellectual disability, Wilson type Cherubism Cryptorchidism-arachnodactyly-intellectual disability syndrome Fibular aplasia-complex brachydactyly syndrome Microform holoprosencephaly Congenital vertical talus, bilateral SLC35A1-CDG Scalp defects-postaxial polydactyly syndrome Brachydactyly-arterial hypertension syndrome Autosomal recessive distal osteolysis syndrome X-linked epilepsy-learning disabilities-behavior disorders syndrome Rare endocrine disease Brachydactyly-short stature-retinitis pigmentosa syndrome Hoyeraal-Hreidarsson syndrome Angelman syndrome due to paternal uniparental disomy of chromosome 15 Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome Cloverleaf skull-asphyxiating thoracic dysplasia syndrome Non-syndromic polydactyly Holoprosencephaly-radial heart renal anomalies syndrome X-linked spinocerebellar ataxia type 4 Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1 Osteomesopyknosis X-linked intellectual disability, Cabezas type Wilson-Turner syndrome Craniosynostosis-dental anomalies X-linked centronuclear myopathy Brachydactyly-preaxial hallux varus syndrome Torg-Winchester syndrome Kleefstra syndrome due to a point mutation Nicolaides-Baraitser syndrome Simpson-Golabi-Behmel syndrome type 2 Bohring-Opitz syndrome Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome Prader-Willi syndrome due to translocation Grant syndrome Septopreoptic holoprosencephaly Male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome Larsen-like osseous dysplasia-short stature syndrome Microcephalic primordial dwarfism, Toriello type 15q13.3 microdeletion syndrome Osteopathia striata-pigmentary dermopathy-white forelock syndrome X-linked intellectual disability-seizures-psoriasis syndrome HSD10 disease, atypical type Carney complex-trismus-pseudocamptodactyly syndrome Lethal Larsen-like syndrome Rare developmental defect during embryogenesis Proximal 16p11.2 microduplication syndrome Lissencephaly Arthrogryposis-like hand anomaly-sensorineural deafness syndrome Exostoses-anetodermia-brachydactyly type E syndrome Polydactyly-myopia syndrome Frontometaphyseal dysplasia Corpus callosum agenesis-abnormal genitalia syndrome Osteopetrosis and related disorders Humeral agenesis/hypoplasia, bilateral ADNP syndrome Rolandic epilepsy-speech dyspraxia syndrome Acromelic frontonasal dysplasia Osteoglosphonic dysplasia Anauxetic dysplasia X-linked spinocerebellar ataxia type 3 Autosomal dominant hypophosphatemic rickets Ulnar hemimelia, bilateral Humero-radial synostosis, unilateral Parastremmatic dwarfism X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome Rare sucking/swallowing disorder Camptodactyly-tall stature-scoliosis-hearing loss syndrome Absent tibia-polydactyly-arachnoid cyst syndrome ANK3-related intellectual disability-sleep disturbance syndrome Parietal foramina with clavicular hypoplasia Cutis gyrata-acanthosis nigricans-craniosynostosis syndrome Grubben-de Cock-Borghgraef syndrome Rhizomelic chondrodysplasia punctata type 3 Orofaciodigital syndrome type 5 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia X-linked hypophosphatemia X-linked intellectual disability, Brooks type Sheldon-Hall syndrome ALG11-CDG Microbrachycephaly-ptosis-cleft lip syndrome Oliver syndrome Spondyloepimetaphyseal dysplasia congenita, Strudwick type Hypomyelination-congenital cataract syndrome Tibial aplasia-ectrodactyly syndrome Goodman syndrome Laryngeal abductor paralysis-intellectual disability syndrome Intellectual disability-alacrima-achalasia syndrome Monoamine oxidase A deficiency X-linked spondyloepimetaphyseal dysplasia Cohen syndrome Platyspondylic dysplasia, Torrance type Prader-Willi syndrome due to imprinting mutation Feingold syndrome type 1 Osteopetrosis with renal tubular acidosis Preaxial polydactyly-colobomata-intellectual disability syndrome Short stature-intellectual disability-eye anomalies-cleft lip/palate syndrome Hutchinson-Gilford progeria syndrome Chondrodysplasia-difference of sex development syndrome Pelizaeus-Merzbacher disease, connatal form Laurence-Moon syndrome X-linked intellectual disability, Gu type Arthrogryposis multiplex congenita-whistling face syndrome Lethal osteosclerotic bone dysplasia Craniofacial conodysplasia Hypoplastic tibiae-postaxial polydactyly syndrome Developmental and speech delay due to SOX5 deficiency Isolated congenital digital clubbing Osteoporosis-pseudoglioma syndrome Early-onset parkinsonism-intellectual disability syndrome Mammary-digital-nail syndrome 3MC syndrome 8q21.11 microdeletion syndrome Blepharophimosis-intellectual disability syndrome, MKB type Mesomelic dysplasia, Savarirayan type Pitt-Hopkins-like syndrome Legg-Calvé-Perthes disease Lateral meningocele syndrome Intellectual disability-seizures-macrocephaly-obesity syndrome Dacryocystitis-osteopoikilosis syndrome Syndactyly-telecanthus-anogenital and renal malformations syndrome Spondyloepimetaphyseal dysplasia, Shohat type Trichorhinophalangeal syndrome type 1 Neonatal Marfan syndrome Familial digital arthropathy-brachydactyly Yunis-Varon syndrome Cornelia de Lange syndrome Arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome Mesomelic dysplasia, Kantaputra type Lethal faciocardiomelic dysplasia X-linked intellectual disability, Snyder type Spondyloepimetaphyseal dysplasia, Missouri type Microcephalic osteodysplastic dysplasia, Saul-Wilson type 15q overgrowth syndrome Thanatophoric dysplasia Fibrodysplasia ossificans progressiva Familial chondromalacia patellae Ulna metaphyseal dysplasia syndrome Microcephaly-seizures-intellectual disability-heart disease syndrome CHIME syndrome Radio-ulnar synostosis, bilateral Brachymorphism-onychodysplasia-dysphalangism syndrome Pseudohypoparathyroidism type 1A Hallux varus-preaxial polysyndactyly syndrome Feingold syndrome type 2 Temtamy preaxial brachydactyly syndrome Distal triplication 15q Brachyolmia Thrombocythemia with distal limb defects POMT2-related limb-girdle muscular dystrophy R14 Severe intellectual disability and progressive spastic paraplegia Microcephaly-cleft palate-abnormal retinal pigmentation syndrome Endocrine-cerebro-osteodysplasia syndrome IMAGe syndrome Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome X-linked congenital disorder of glycosylation with intellectual disability as a major feature SPONASTRIME dysplasia Pseudopseudohypoparathyroidism Microcephaly-cervical spine fusion anomalies syndrome Lenz-Majewski hyperostotic dwarfism Intellectual disability-myopathy-short stature-endocrine defect syndrome X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome Pseudoachondroplasia Hip dysplasia, Beukes type Pachydermoperiostosis Astley-Kendall dysplasia Spondyloepimetaphyseal dysplasia with joint laxity Aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome Spondylo-megaepiphyseal-metaphyseal dysplasia Stüve-Wiedemann syndrome Hypoxanthine-guanine phosphoribosyltransferase deficiency Harrod syndrome 17q21.31 microduplication syndrome Symbrachydactyly of hands and feet Infantile osteopetrosis with neuroaxonal dysplasia FOXP1 Syndrome White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome 19p13.13 microdeletion syndrome Congenital muscular dystrophy with intellectual disability and severe epilepsy Costello syndrome Weismann-Netter syndrome Radio-ulnar synostosis, unilateral Intermediate osteopetrosis Talo-patello-scaphoid osteolysis Osteonecrosis Bone dysplasia, Azouz type Crossed polysyndactyly X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome Mowat-Wilson syndrome due to monosomy 2q22 Inverse Klippel-Trénaunay syndrome Blomstrand lethal chondrodysplasia Congenital elbow dislocation, bilateral Congenital pseudoarthrosis of the clavicle Autosomal dominant popliteal pterygium syndrome X-linked skeletal dysplasia-intellectual disability syndrome Osteonecrosis of the jaw Limb-mammary syndrome Mosaic monosomy X Microlissencephaly-micromelia syndrome B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome STT3B-CDG Microcephaly-microcornea syndrome, Seemanova type Summitt syndrome X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome Perinatal lethal hypophosphatasia Intellectual disability-short stature-hypertelorism syndrome PMM2-CDG Lipodystrophy-intellectual disability-deafness syndrome Tall stature-long halluces-multiple extra-epiphyses syndrome Zellweger-like syndrome without peroxisomal anomalies Diaphyseal medullary stenosis-bone malignancy syndrome Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Spondyloepimetaphyseal dysplasia, Handigodu type Severe intellectual disability-progressive spastic diplegia syndrome X-linked intellectual disability with isolated growth hormone deficiency Pelizaeus-Merzbacher disease, classic form Deafness-intellectual disability syndrome, Martin-Probst type W syndrome Familial avascular necrosis of femoral head Frank-Ter Haar syndrome X-linked intellectual disability-psychosis-macroorchidism syndrome X-linked intellectual disability-macrocephaly-macroorchidism syndrome Distal arthrogryposis type 5D Feingold syndrome Severe X-linked intellectual disability, Gustavson type Craniometadiaphyseal dysplasia, wormian bone type Rare syndromic intellectual disability Microcephaly-deafness-intellectual disability syndrome X-linked intellectual disability, Seemanova type Buschke-Ollendorff syndrome Femoral-facial syndrome Hypospadias-intellectual disability, Goldblatt type syndrome STT3A-CDG Tricho-dento-osseous syndrome X-linked intellectual disability, Pai type Non syndromic limb overgrowth Diaphanospondylodysostosis Saldino-Mainzer syndrome Blepharophimosis-intellectual disability syndrome, Verloes type GM3 synthase deficiency Endosteal sclerosis-cerebellar hypoplasia syndrome Rare skin disease 17q11.2 microduplication syndrome X-linked intellectual disability, Stoll type Walker-Warburg syndrome Primary avascular necrosis Disorders of vitamin D metabolism Metaphyseal dysplasia, Braun-Tinschert type X-linked intellectual disability, Shrimpton type Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria Familial hypocalciuric hypercalcemia type 1 Intellectual disability-polydactyly-uncombable hair syndrome MAN1B1-CDG Spondyloenchondrodysplasia Neurofaciodigitorenal syndrome Brachydactyly-long thumb syndrome Diastrophic dysplasia Fountain syndrome Singleton-Merten dysplasia X-linked intellectual disability, Turner type Ptosis-syndactyly-learning difficulties syndrome Premature chromosome condensation with microcephaly and intellectual disability Caffey disease Finger hyperphalangy-toe anomalies-severe pectus excavatum syndrome Triphalangeal thumbs-brachyectrodactyly syndrome Craniofaciofrontodigital syndrome Pyruvate dehydrogenase deficiency X-linked intellectual disability-acromegaly-hyperactivity syndrome Humero-ulnar synostosis X-linked progressive cerebellar ataxia Hemimelia Kienbock disease Neurofibromatosis type 1 due to NF1 mutation or intragenic deletion Idiopathic juvenile osteoporosis Charcot-Marie-Tooth disease-deafness-intellectual disability syndrome Neuroectodermal-endocrine syndrome X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome ALG1-CDG Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature Full schwannomatosis Congenital genu flexum Metaphyseal anadysplasia Intellectual disability-seizures-hypophosphatasia-ophthalmic-skeletal anomalies syndrome Phosphoribosylpyrophosphate synthetase superactivity Calvarial doughnut lesions-bone fragility syndrome Mucopolysaccharidosis type 2, severe form Williams syndrome X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome Alobar holoprosencephaly X-linked intellectual disability-retinitis pigmentosa syndrome Thanatophoric dysplasia type 1 Otopalatodigital syndrome type 1 Deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome Spondylo-ocular syndrome Familial expansile osteolysis Traumatic avascular necrosis 12q14 microdeletion syndrome Primary bone dysplasia with progressive ossification of skin, skeletal muscle, fascia, tendons and ligaments Macrodactyly of toes, unilateral Cleidocranial dysplasia Spastic paraplegia-epilepsy-intellectual disability syndrome Craniosynostosis-intracranial calcifications syndrome X-linked neurodegenerative syndrome, Bertini type Mazabraud syndrome CHST3-related skeletal dysplasia Hypomyelination neuropathy-arthrogryposis syndrome Sinding-Larsen-Johansson disease Panner disease Dysspondyloenchondromatosis Cleidorhizomelic syndrome Madelung deformity Osgood-Schlatter disease Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency Genochondromatosis type 1 Midline interhemispheric variant of holoprosencephaly Hennekam syndrome Spastic paraplegia-glaucoma-intellectual disability syndrome Ulnar/fibula ray defect-brachydactyly syndrome X-linked neurodegenerative syndrome, Hamel type Mowat-Wilson syndrome due to a ZEB2 point mutation 15q24 microdeletion syndrome Lowry-MacLean syndrome Intellectual disability-obesity-brain malformations-facial dysmorphism syndrome COG8-CDG Brachydactyly type A6 Ischiovertebral syndrome Fried syndrome Primary intraosseous venous malformation Trigonocephaly-broad thumbs syndrome Autism spectrum disorder-epilepsy-arthrogryposis syndrome Craniosynostosis-anal anomalies-porokeratosis syndrome Acheiria, bilateral Idiopathic avascular necrosis Hernández-Aguirre Negrete syndrome Guttmacher syndrome Rare urogenital disease Keutel syndrome Non-syndromic metopic craniosynostosis X-linked intellectual disability-ataxia-apraxia syndrome Rare systemic or rheumatologic disease Arthrogryposis-anterior horn cell disease syndrome Brachydactyly type C Lujan-Fryns syndrome Secondary avascular necrosis Hereditary bullous dystrophy, macular type Hypocalcemic rickets Oculoauriculovertebral spectrum with radial defects Autosomal recessive spastic paraplegia type 11 X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome Severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia Hereditary hypophosphatemic rickets with hypercalciuria Hunter-McAlpine syndrome Deafness-onychodystrophy syndrome Genitopatellar syndrome Primary bone dysplasia Brachydactyly type A1 Apodia, unilateral Paraplegia-brachydactyly-cone-shaped epiphysis syndrome Trigonocephaly-short stature-developmental delay syndrome Intellectual disability-hyperkinetic movement-truncal ataxia syndrome Acropectoral syndrome Ramos-Arroyo syndrome Brachydactyly type E Spondyloepiphyseal dysplasia congenita Acrocephalopolydactyly Osteochondrosis Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome Monosomy 22q13.3 Optic atrophy-intellectual disability syndrome Acrocardiofacial syndrome X-linked Charcot-Marie-Tooth disease Adactyly of foot, bilateral Ear-patella-short stature syndrome S-adenosylhomocysteine hydrolase deficiency Subependymal nodular heterotopia Terminal transverse defects of arm Craniosynostosis, Herrmann-Opitz type Sub-cortical nodular heterotopia Rare circulatory system disease X-linked Charcot-Marie-Tooth disease type 6 Lesch-Nyhan syndrome Otopalatodigital syndrome spectrum disorder Coffin-Siris syndrome THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome Pfeiffer syndrome type 1 Microcephaly-thin corpus callosum-intellectual disability syndrome Chondrodysplasia punctata, tibial-metacarpal type Brachydactyly type A4 Brain malformation-congenital heart disease-postaxial polydactyly syndrome Dyggve-Melchior-Clausen disease Brachytelephalangic chondrodysplasia punctata Orofaciodigital syndrome Microphthalmia-brain atrophy syndrome Spondylometaphyseal dysplasia, Golden type Nodular neuronal heterotopia Rhizomelic dysplasia, Patterson-Lowry type Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome Brachydactyly type A2 Maffucci syndrome Pfeiffer syndrome type 3 Secondary non-traumatic avascular necrosis Infantile hypophosphatasia Pfeiffer syndrome type 2 Renpenning syndrome Sporadic infantile bilateral striatal necrosis Orofaciodigital syndrome type 11 Cleft palate-short stature-vertebral anomalies syndrome Mowat-Wilson syndrome HSD10 disease Congenital muscular dystrophy with cerebellar involvement Arthrogryposis-renal dysfunction-cholestasis syndrome Wrinkly skin syndrome Crouzon syndrome-acanthosis nigricans syndrome Brachydactyly type A7 Rare otorhinolaryngologic disease Familial infantile bilateral striatal necrosis Distal deletion 6p Axial spondylometaphyseal dysplasia Syndromic multisystem autoimmune disease due to Itch deficiency Juvenile sialidosis type 2 Hamel cerebro-palato-cardiac syndrome 48,XXXY syndrome Epiphysiolysis of the hip Tetramelic monodactyly X-linked intellectual disability, Porteous type Guanidinoacetate methyltransferase deficiency Symphalangism with multiple anomalies of hands and feet Postaxial acrofacial dysostosis Femur-fibula-ulna complex Autosomal dominant otospondylomegaepiphyseal dysplasia Polymicrogyria Humerus trochlea aplasia Hypotonia-speech impairment-severe cognitive delay syndrome Hirsutism-skeletal dysplasia-intellectual disability syndrome Bilateral polymicrogyria DPAGT1-CDG Partington syndrome Female restricted epilepsy with intellectual disability Pelvis-shoulder dysplasia Distal symphalangism X-linked intellectual disability, Golabi-Ito-Hall type Syndactyly type 4 Saethre-Chotzen syndrome Pelvic dysplasia-arthrogryposis of lower limbs syndrome Atelosteogenesis type III Cardiofaciocutaneous syndrome Robinow syndrome Syndactyly type 2 Proximal symphalangism Mucopolysaccharidosis type 2, attenuated form 3C syndrome Amelia Dysostosis 48,XXYY syndrome Intercalary limb defects Achondroplasia Split hand or/and split foot malformation Terminal limb defects Adactyly of hand Muenke syndrome Postaxial polydactyly of fingers Acrofacial dysostosis Dysostosis with limb anomaly as a major feature Brachydactyly Dysostosis with limb and face anomalies as a major feature Preaxial polydactyly of fingers Joint formation defects Congenital joint dislocations Intellectual disability-brachydactyly-Pierre Robin syndrome Acrocallosal syndrome Congenital deformities of limbs Congenital deformities of fingers Mandibuloacral dysplasia with type A lipodystrophy Acromesomelic dysplasia, Maroteaux type Dysostosis with combined reduction defects of upper and lower limbs Mandibuloacral dysplasia with type B lipodystrophy Syndrome with limb duplication, polydactyly, syndactyly, and/or hyperphalangy Adenylosuccinate lyase deficiency Syndrome with limb reduction defects Lethal congenital contracture syndrome Aicardi syndrome Aicardi-Goutières syndrome Amelia of upper limb Albers-Schönberg osteopetrosis Popliteal pterygium syndrome Humeral agenesis/hypoplasia Allan-Herndon-Dudley syndrome Congenital absence of upper arm and forearm with hand present Amelia of lower limb Tetra-amelia Congenital absence of both lower leg and foot Acheiria Congenital absence of thigh and lower leg with foot present Congenital absence of both forearm and hand Angelman syndrome Congenital hypoplasia of thumb Gorham-Stout disease Apodia Brachydactyly of toes Split hand Apert syndrome Preaxial polydactyly of toes Constriction rings syndrome Syndactyly type 6 Familial isolated clinodactyly of fingers Postaxial polydactyly of toes Congenital pseudoarthrosis of the fibula Camptodactyly of fingers Congenital patella dislocation Borjeson-Forssman-Lehmann syndrome Macrodactyly of fingers X-linked intellectual disability, Cilliers type Syndromic craniosynostosis Congenital absence of upper arm and forearm with hand present, unilateral Congenital absence of upper arm and forearm with hand present, bilateral Fibular hemimelia, unilateral Alazami syndrome Cockayne syndrome type 3 Autosomal recessive cutis laxa type 2 Léri-Weill dyschondrosteosis Fibrous dysplasia of bone Central polydactyly of fingers, bilateral 17p13.3 microduplication syndrome Metaphyseal chondrodysplasia, Jansen type Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome Aphalangy-syndactyly-microcephaly syndrome Neurogenic arthrogryposis multiplex congenita Infantile-onset X-linked spinal muscular atrophy Arthrogryposis due to muscular dystrophy Progressive pseudorheumatoid arthropathy of childhood Pyruvate dehydrogenase E1-beta deficiency Congenital absence/hypoplasia of fingers excluding thumb Brachydactyly of fingers Antley-Bixler syndrome Fanconi anemia Split foot Central polydactyly Hyperphalangy Bannayan-Riley-Ruvalcaba syndrome Congenital pseudoarthrosis of the tibia Tibio-fibular synostosis Auriculoosteodysplasia True congenital shoulder dislocation Congenital contractural arachnodactyly Congenital pseudoarthrosis of the radius X-linked intellectual disability, Nascimento type Congenital pseudoarthrosis of the ulna Patella aplasia/hypoplasia, unilateral X-linked cerebral-cerebellar-coloboma syndrome Isolated congenital radial head dislocation X-linked dominant chondrodysplasia, Chassaing-Lacombe type Macrodactyly of toes Patella aplasia/hypoplasia, bilateral X-linked cerebral adrenoleukodystrophy X-linked intellectual disability-craniofacioskeletal syndrome Amelia of upper limb, unilateral X-linked intellectual disability, Van Esch type CHILD syndrome Amelia of upper limb, bilateral Campomelic dysplasia X-linked intellectual disability-spastic quadriparesis syndrome Upper limb hypertrophy Lower limb hypertrophy Humeral agenesis/hypoplasia, unilateral Amelia of lower limb, unilateral Developmental delay-deafness syndrome, Hildebrand type Amelia of lower limb, bilateral Radial hemimelia, unilateral Radial hemimelia, bilateral Femoral agenesis/hypoplasia, bilateral X-linked syndromic intellectual disability Tibial hemimelia, unilateral Tibial hemimelia, bilateral Ulnar hemimelia, unilateral Fibular hemimelia, bilateral Non-rhizomelic chondrodysplasia punctata Rhizomelic chondrodysplasia punctata Congenital absence of both forearm and hand, unilateral Congenital absence of both forearm and hand, bilateral Congenital absence of thigh and lower leg with foot present, unilateral Congenital absence of thigh and lower leg with foot present, bilateral Arthrogryposis-severe scoliosis syndrome Acheiria, unilateral Congenital absence of both lower leg and foot, unilateral Cockayne syndrome Congenital absence of both lower leg and foot, bilateral Microcephalic primordial dwarfism, Dauber type Coffin-Lowry syndrome Parkes Weber syndrome Klippel-Trénaunay syndrome Apodia, bilateral Adactyly of foot, unilateral Autosomal dominant multiple pterygium syndrome Crouzon syndrome Cockayne syndrome type 1 Cockayne syndrome type 2 ISPD-related limb-girdle muscular dystrophy R20 Carpenter syndrome Hyperphalangy, unilateral Hyperphalangy, bilateral Digital anomalies-intellectual disability-short stature syndrome Symbrachydactyly of hand and foot, unilateral Dubowitz syndrome Autism spectrum disorder due to AUTS2 deficiency Nager syndrome Multiple epiphyseal dysplasia 19q13.11 microdeletion syndrome Preaxial polydactyly of toes, unilateral Central polydactyly of fingers, unilateral Preaxial polydactyly of toes, bilateral Zygodactyly type 2 Zygodactyly type 1 Synpolydactyly type 2 Oncogenic osteomalacia Synpolydactyly type 3 Zygodactyly type 4 Ellis Van Creveld syndrome Humero-radio-ulnar synostosis, unilateral Microduplication Xp11.22p11.23 syndrome Humero-radio-ulnar synostosis, bilateral Congenital vertical talus, unilateral Ollier disease Humero-ulnar synostosis, unilateral Macrocephaly-developmental delay syndrome Humero-ulnar synostosis, bilateral Humero-radial synostosis, bilateral Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome Madelung deformity, unilateral Déformation de Madelung bilatérale Genu recurvatum congénital Luxation congénitale du coude, unilatérale Maladie des exostoses multiples Luxation congénitale de la rotule, bilatérale Macrodactylie des doigts, unilatérale Syndrome de Bainbridge-Ropers Luxation congénitale de la rotule, unilatérale Macrodactylie des orteils, bilatérale Macrodactylie des doigts, bilatérale Forme létale du syndrome des ptérygiums multiples Syndrome de Simpson-Golabi-Behmel Syndrome de Goldenhar Syndrome de Gordon Syndrome de microdélétion 3q27.3 Syndrome microgéodique des phalanges Syndrome de céphalopolysyndactylie de Greig Syndrome de Holt-Oram Hypercalcémie hypocalciurique familiale Syndrome de Joubert avec dystrophie thoracique asphyxiante de Jeune Syndrome de dysmorphie craniofaciale-anomalies squelettiques-cardiopathie-trouble neurologique du développement dû à une microdélétion 9q21.3 Hypophosphatasie Rachitisme hypophosphatémique Dysplasie gnatho-diaphysaire Syndrome de Prader-Willi dû à une disomie uniparentale maternelle du chromosome 15 Lissencéphalie liée à l'X avec anomalies génitales Incontinentia pigmenti Syndrome de Jeune Dysplasie de Kniest Syndrome d'alpha-thalassémie-déficience intellectuelle associée au chromosome 16 Syndrome de Prader-Willi dû à une délétion 15q11q13 d'origine paternelle Syndrome trichorhinophalangien type 2 Syndrome de Larsen Syndrome de dysplasie spondylo-métaphysaire-hypotrichose Syndrome de dysplasie spondylo-épimétaphysaire-dentition anormale Dysplasie spondylo-épimétaphysaire type Geneviève Syndrome de Stickler type 1 Syndrome oto-palato-digital type 2 Syndrome de Stickler type 2 Syndrome de Marfan Syndrome de Marshall Syndrome de Meckel Maladie de Menkes Syndrome de Temple Syndrome de Temple lié à une hypométhylation paternelle 14q32.2 Mucopolysaccharidose type 2 Polymicrogyrie bilatérale périsylvienne Atrophie optique précoce liée à l'X Dysplasie spondylo-métaphysaire type A4 Syndrome de dysplasie spondylo-métaphysaire-avant-bras incurvé-dysmorphie faciale Syndrome de déficience intellectuelle sévère-microcéphalie postnatale progressive-stéréotypies manuelles sur la ligne médiane Syndrome de Nance-Horan Neurofibromatose type 1 Schwannomatose liée à NF2 germinale Maladie de Norrie Syndrome de déficience intellectuelle-obésité-prognathisme-anomalies oculaires et cutanées Syndrome d'Ondine Déficit en ornithine transcarbamylase Ostéopétrose maligne autosomique récessive Syndrome de Pallister-Hall Dysplasie de la tête du fémur type Meyer Maladie de Pelizaeus-Merzbacher Cutis laxa autosomique récessive type 2A Glycogénose par déficit en phosphoglycérate kinase 1 Cutis laxa autosomique récessive type 2 classique Syndrome de Prader-Willi Syndrome de Prader-Willi-like associé à MAGEL2 Pycnodysostose Syndrome d'ulna courte-dysmorphie-hypotonie-déficience intellectuelle Syndrome oculo-auriculo-fronto-nasal Syndrome de Townes-Brocks Syndrome cardiomélique type slovène Syndrome de Turner Syndrome de l'X fragile Monosomie X Acheiropodie Acrodysostose Dysplasie acromésomélique type Hunter-Thompson Syndrome d'Adams-Oliver Syndrome ADULT Syndrome d'hypoglossie-hypodactylie Syndrome d'alopécie-contractures-nanisme-déficience intellectuelle Syndrome de Rubinstein-Taybi dû à des mutations de CREBBP Syndrome de Rubinstein-Taybi dû à une microdélétion 16p13.3 Arthrogrypose multiple congénitale Syndrome d'aniridie-ataxie cérébelleuse-déficience intellectuelle Syndrome d'aniridie-déficience intellectuelle Syndrome d'ankylose des pouces-brachydactylie-déficience intellectuelle Scaphocéphalie familiale type McGillivray Maladie de Charcot-Marie-Tooth liée à l'X type 5 Cutis laxa autosomique récessive type 2B Syndrome d'incurvation latérale sévère du tibia-petite taille-omoplate ailée modérée-dysmorphie faciale modérée Aplasie/hypoplasie de la rotule Syndrome de Smith-Lemli-Opitz Encéphalopathie épileptique à début précoce et déficience intellectuelle liées à une mutation de GRIN2A Microphtalmie avec défauts linéaires cutanés Syndrome de Mononen-Karnes-Senac Syndrome de Myhre Syndrome nail-patella Nanisme microcéphalique primordial type Montréal Dysplasie métatropique Nanisme microcéphalique ostéodysplasique primordial types I et III Syndrome de déficience intellectuelle liée à l'X-hypoplasie cérébelleuse Syndrome d'Okamoto Syndrome d'insuffisance pancréatique-anémie-hyperostose Syndrome d'Opitz GBBB Syndrome oro-facio-digital type 3 Polymicrogyrie unilatérale hémisphérique Maladie de Nasu-Hakola Maladie de Charcot-Marie-Tooth liée à l'X type 3 Syndrome d'ostéoporose-hypopigmentation oculocutanée Hyperostose endostéale type Worth Anomalie chromosomique rare Syndrome de Furhmann Syndrome de petite taille-pterygium colli-cardiopathie congénitale Syndrome cardio-crânien type Pfeiffer Phocomélie type Schinzel Syndrome de déficience intellectuelle liée à l'X-plagiocéphalie Syndrome d'agénésie du corps calleux-déficience intellectuelle-colobome-micrognathie Syndrome de polyneuropathie-déficience intellectuelle-acromicrie-ménopause prématurée Syndrome de pouce triphalangé-polysyndactylie Syndrome d'Ehlers-Danlos musculocontractural Pseudoprogéria Maladie de Pyle Syndrome de déficience intellectuelle-cataracte-calcification du pavillon auriculaire-myopathie Syndrome de déficience intellectuelle-microcéphalie-anomalies phalangiennes et faciales Déficience intellectuelle type Buenos-Aires Déficience intellectuelle type Wolff Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle par déficit de TUD Syndrome de Rett atypique Syndrome de Richieri-Costa-da Silva Syndrome de Robinow autosomique dominant Maladie de Scheuermann Syndrome des côtes courtes-polydactylie type Majewski Dysplasie fibreuse polyostotique Trouble neurologique du développement associé à CTCF Syndrome de spasticité-déficience intellectuelle-épilepsie lié à l'X Anomalie rare du développement osseux d'origine génétique Brachyolmie type 1 de Hobaek Dysplasie épiphysaire multiple type 5 Dysplasie spondylo-métaphysaire type Kozlowski Omodysplasie autosomique récessive Syndrome des synostoses multiples Dysplasie pseudodiastrophique Syndrome de syndactylie-polydactylie-lobe d'oreille anormal Syndrome de Rett Syndrome de Goldberg-Shprintzen avec mégacôlon Syndrome d'Atkin-Flaitz Chondrodysplasie métaphysaire type Kaitila Syndrome d'hypoplasie du cubitus-déficience intellectuelle Syndrome d'hypoplasie du pouce-alopécie-anomalie de la pigmentation Cancer du sein héréditaire Syndrome d'ichtyose-alopécie-éclabion-ectropion-déficience intellectuelle Incisive centrale maxillaire médiane unique XYLT1-CDG Syndrome salt-and-pepper Syndrome ANE Syndrome de Johanson-Blizzard Syndrome neuroectodermique de Johnson Syndrome Kabuki Syndrome de Sanjad-Sakati Pied bot familial dû à une mutation ponctuelle de PITX1 Craniosynostose bicoronale non syndromique Syndrome KBG Syndrome de kératose folliculaire-nanisme-atrophie cérébrale Syndrome de Marfan type 2 Dysplasie létale Kniest-like Syndrome Patterson-Stevenson-Fontaine Syndrome MASA Syndrome FATCO Syndrome de microcéphalie-cardiomyopathie Syndrome de Rubinstein-Taybi Dystrophie musculaire des ceintures associée à POMT1 R11 Syndrome de dysostose mandibulo-faciale-macroblépharon-macrostomie Sclérose tubéreuse de Bourneville Syndrome CEDNIK Atélostéogenèse type I Sacophocépalie syndromique familiale Syndrome blépharo-naso-facial Dysplasie en boomerang Syndrome de spasmes infantiles-retard psychomoteur-atrophie cérébrale progressive-anomalie des ganglions de la base Syndrome Aymé-Gripp Syndrome de brachydactylie-dysplasie des coudes et des poignets Syndrome de brachydactylie-mésomélie-déficience intellectuelle-malformations cardiaques Syndrome d'Eiken Syndrome de brachytéléphalangie-dysmorphie-syndrome de Kallman Syndrome C Campomélie type Cumming Camptobrachydactylie Maladie de Camurati-Engelmann COG5-CDG Dysplasie diaphysaire tachetée Cheiro-spondylo-enchondromatose Dysplasie spondylo-épiphysaire type Maroteaux Syndrome cardiomélique type 2 COG4-CDG Syndrome de cardiopathie congénitale-face ronde-petite taille Syndrome de déficience intellectuelle-dysmorphie faciale-anomalies des mains Syndrome de cataracte-hypertrichose-déficience intellectuelle Syndrome d'ataxie-déficience intellectuelle-apraxie oculomotrice-kystes cérébelleux Syndrome de cataracte-néphropathie-encéphalopathie Syndrome de Catel-Manzke Syndrome de cécité corticale-déficience intellectuelle-polydactylie Syndrome cérébrocostomandibulaire Syndrome d'aplasie du cervelet-hydrocéphalie Ostéochondrite disséquante familiale Syndrome Charlie M Déficit partiel en hypoxanthine guanine phosphoribosyltransférase Syndrome d'anomalie des cheveux-photosensibilité-déficience intellectuelle Syndrome de coalition tarso-carpienne Chondrodysplasie létale type Moerman Déficit en pyruvate déshydrogénase E2 Chondrodysplasie létale type Seller Déficit en phosphatase du complexe pyruvate déshydrogénase Chondrodysplasie létale autosomique récessive Syndrome de Desbuquois Dysplasie squelettique létale type Greenberg Dysplasie oto-spondylo-mégaépiphysaire Syndrome du chromosome 10 en anneau Syndrome COFS Syndrome de colobome-fente labiopalatine-déficience intellectuelle Syndrome de contractures-dysplasie ectodermique-fente labiopalatine Syndrome des contractures congénitales létales type 1 ALG3-CDG Agénésie complexe du corps calleux liée à l'X MPDU1-CDG ALG8-CDG Syndrome d'hyperphosphatasie-déficience intellectuelle Syndrome CDG-ALG2 MGAT2-CDG Syndrome des côtes courtes-polydactylie Syndrome de Robinow autosomique récessif Syndrome coxo-auriculaire Syndrome de Crane-Heise Dysplasie cranio-ectodermique Syndrome de Cantú Syndrome d'hypertélorisme associé à SPECC1L Syndrome de Larsen-like de type B3GAT3 Chondrodysplasie ponctuée type Sheffield Chondrodysplasie ponctuée type Toriello Syndrome CK Syndrome cranio-micromélique Dysplasie cranio-télencéphalique Syndrome de craniosynostose-cataracte Craniosynostose Syndrome de craniosynostose-brachydactylie Nanisme primordial microcéphalique par déficit en ZNF335 Syndrome de déficience intellectuelle-dysmorphie craniofaciale-cryptorchidie Syndrome de Currarino Syndrome de duplication Xp22.13p22.2 Syndrome de Curry-Jones Polymicrogyrie due à une mutation TUBB2B Syndrome de Dandy-Walker-polydactylie postaxiale Syndrome de dysostose spondylocostale-hypospadias-déficience intellectuelle Syndrome de blépharophimosis-déficience intellectuelle par déficit en UBE3B Nécrose striatale bilatérale de l'enfant Délétion distale 3p Pseudohypoparathyroïdie type 1C Forme létale liée à l'X du syndrome des ptérygiums multiples Syndrome de mains et pieds fendus-surdité Brachydactylie type B2 Arthrogrypose distale type 10 Syndrome de synostose radio-ulnaire-thrombocytopénie amégacaryocytique Dysplasie cranio-lenticulo-suturale Syndrome de Wolcott-Rallison Maladie de Pelizaeus-Merzbacher chez les femmes porteuses Maladie de Pelizaeus-Merzbacher, forme transitoire Duplication distale 15q Maladie de Pelizaeus-Merzbacher par mutation non-sens de PLP1 Syndrome de dyschondrostéose-néphropathie Syndrome de Temtamy Syndrome de Prader-Willi dû à une délétion 15q11q13 d'origine paternelle de type 2 Syndrome angio-ostéo-hypotrophique Dysostose acrofaciale type Palagonia Dysostose acrofaciale type Rodríguez Déficit en glycérol kinase, forme infantile Dysostose oculo-maxillo-faciale Dysostose type Stanescu Syndrome de paraplégie spastique-maladie de Paget Dysplasie kyphomélique Dystrophie musculaire des ceintures liée à l'alpha dystroglycane R16 Dysplasie hémato-diaphysaire de Ghosal Dysplasie thoracomélique Glycogénose par déficit en LAMP-2 Dysplasie épiphysaire hémimélique Syndrome de Lowry-Wood Dysplasie immuno-osseuse de Schimke Dysplasie osseuse létale type Holmgren-Forsell Nécrose avasculaire Maladie neurométabolique syndromique avec déficience intellectuelle non liée à l'X Syndrome de dysplasie spondylo-périphérique-cubitus court Syndrome de dysplasie squelettique-épilepsie-petite taille Syndrome de déficience intellectuelle récessive-dysfonctionnement moteur-contractures articulaires multiples Sialidose type 2 Dysplasie dyssegmentaire type Silverman-Handmaker Hypophosphatasie prénatale bénigne Mélorhéostose avec ostéopoecilie Syndrome EEM Hypophosphatasie de l'enfant Syndrome d'Angelman dû à une mutation ponctuelle Syndrome d'Emery-Nelson Syndrome de Kleefstra dû à une microdélétion 9q34 Syndrome d'épilepsie-microcéphalie-dysplasie squelettique Complexe de Gollop-Wolfgang Agénésie/hypoplasie du fémur Syndrome de Pai Dysplasie phalango-épiphysaire en ailes d'anges Fibrochondrogenèse Syndrome de Floating-Harbor Syndrome 49,XXXXY Chondrodysplasie avec luxation articulaire type gPAPP Syndrome de fusion splénogonadique-anomalie transversale des membres-micrognathie Syndrome GAPO Syndrome de glabelle proéminente-microcéphalie-petite taille Hypoplasie dermique en aires Dysplasie acromésomélique type Grebe Syndrome de Hall-Riggs Syndrome de Hallermann-Streiff Syndrome d'anomalies congénitales multiples-hypotonie-épilepsie Acrodysostose avec résistance aux multiples hormones Maladie gynécologique ou obstétrique rare Lissencéphalie type 1 due aux anomalies du gène double-cortine Syndactylie mésoaxiale synostosique avec réduction phalangienne Holoprosencéphalie Pseudoarthrose congénitale des membres Syndrome d'holoprosencéphalie-craniosynostose Hyalinose systémique infantile Hyperostose vertébrale ankylosante avec tylose Syndrome de Seckel Syndrome de Smith-Magenis Syndrome de déficience intellectuelle liée à l'X-cardiomégalie-insuffisance cardiaque congénitale Syndrome d'Aarskog-Scott Dysostose acro-cranio-faciale Dysostose acrofaciale type Weyers Dysplasie acropectorovertébrale Syndrome d'alopécie-épilepsie-pyorrhée-déficience intellectuelle Syndrome d'ostéopénie-myopie-surdité-déficience intellectuelle-dysmorphie Amélie autosomique récessive Maladie des brides amniotiques Anencéphalie/exencéphalie isolée Maladie néoplasique rare Syndrome d'aniridie-ptosis-déficience intellectuelle-obésité Syndrome cérébrooculonasal Syndrome de Roberts Syndrome de dysplasie frontonasale-alopécie-anomalies génitales Syndrome de crâne en trèfle-anomalies congénitales multiples Syndrome des côtes courtes-polydactylie type Beemer-Langer Arthrose précoce avec dysplasie spondyloépiphysaire intermédiaire due à une mutation du gène COL2A1 Dysplasie spondylo-épimétaphysaire type matrilin-3 Syndrome L1 Syndrome de Turner par anomalies de structure du chromosome X Syndrome d'aphalangie-hémivertèbre-dysgénésie uro-génito-intestinale Syndrome d'aplasie du péroné-ectrodactylie Syndrome d'aplasie radiale-aplasie tibiale Syndrome d'arachnodactylie-ossification anormale-déficience intellectuelle Arthrogrypose distale type 1 Syndrome de Kuskokwim Syndrome d'ataxie-surdité-atrophie optique-létalité Syndrome de dysplasie osseuse terminale-défauts de pigmentation Syndrome 3M Dysplasie géléophysique Dysplasie mésomélique type Nievergelt Nanisme microcéphalique ostéodysplasique primordial type II Nanisme micromélique type Fryns Polymicrogyrie unilatérale Pied bot familial avec ou sans autres anomalies des membres inférieurs Dysplasie oculo-dento-digitale Oligodactylie post-axiale tétramélique Omodysplasie Syndrome létal d'omphalocèle-fente palatine Opsismodysplasie Syndrome orofaciodigital type 6 Polymicrogyrie bilatérale frontopariétale Maladie de Blount Syndrome d'ostéopathie striée-sclérose crânienne Ostéopétrose autosomique dominante type 1 Syndrome d'ostéoporose-macrocéphalie-cécité-hyperlaxité articulaire Syndrome de pachygyrie-déficience intellectuelle-épilepsie Maladie de Paget juvénile Syndrome de paraplégie-déficience intellectuelle-hyperkératose Anomalie congénitale des membres Syndrome de Pitt-Hopkins Syndrome de polymicrogyrie-turricéphalie-hypogénitalisme Syndrome des pouces en adduction-arthrogrypose, type Christian Syndrome d'acrodysplasie-scoliose Syndrome de Qazi-Markouizos Syndrome de déficience intellectuelle-dysmorphie-hypogonadisme-diabète sucré Atélostéogenèse type II Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle Syndrome d'ataxie cérébelleuse autosomique récessive-épilepsie-déficience intellectuelle par déficit de RUBCN Syndrome rhizomélique type Urbach Dystrophie musculaire des ceintures associée à GMPPB R19 Dysplasie spondylo-épiphysaire tardive Dysplasie spondylo-métaphysaire type Schmidt Hémimélie cubitale Dysplasie spondylo-épimétaphysaire type Irapa Syndrome d'achondroplasie sévère-retard de développement-acanthosis nigricans Syndrome de dysplasie spondylo-métaphysaire-dystrophie des cônes et des bâtonnets Syndrome de dysplasie spondylo-épimétaphysaire-membres courts-anomalies de calcification Dysplasie spondylo-épimétaphysaire avec hyperlaxité ligamentaire type leptodactylique Synostose huméro-radiale Synostose huméro-radio-cubitale Synostose lambdoïde familiale Syndrome de synostose radio-ulnaire-microcéphalie-scoliose Brachydactylie type B Synostose spondylo-carpo-tarsienne Brachydactylie type A5 Syndrome de nodulose-arthropathie-ostéolyse Syndrome de Ballard Génochondromatose type 2 Sialidose type 2 congénitale Syndactylie type 1 Syndactylie type 3 Dysplasie thoraco-laryngo-pelvienne Dysplasie avec gracilité osseuse Déficience intellectuelle liée à l'X type Cantagrel Syndrome de déficience intellectuelle liée à l'X-cubitus valgus-dysmorphie Déficience intellectuelle liée à l'X type Siderius Syndrome de trismus-pseudocamptodactylie Syndrome de déficience intellectuelle liée à l'X-puberté précoce-obésité Déficience intellectuelle liée à l'X type Stevenson Syndrome d'Urban-Rogers-Meyer Déficience intellectuelle liée à l'X type Zorick Syndrome de Woodhouse-Sakati Syndrome de Zimmermann-Laband Syndrome d'Opitz G/BBB lié à l'X Syndrome de déficience intellectuelle liée à l'X-faciès hypotonique Syndrome d'anomalies de l'ossification-retard psychomoteur Syndrome de neuropathie viscérale-anomalies cérébrales-dysmorphie-retard du développement Syndrome de microcéphalie-polymicrogyrie-agénésie du corps calleux Holoprosencéphalie lobaire Infertilité rare Déficience intellectuelle liée à l'X type Sutherland-Haan Déficience intellectuelle liée à l'X type Hedera Syndrome de Juberg-Marsidi Ostéite condensante médiane de la clavicule Dysplasie osseuse primaire avec micromélie Ostéoporose liée à l'X avec fractures Dysplasie de Smith-McCort Hypotrichose-déficience intellectuelle, type Lopes Déficience intellectuelle type Birk-Barel Syndrome de dysmorphie-petite taille-surdité-différence du développement sexuel Syndrome d'incurvation congénitale des os longs-petite taille-dolichomacrocéphalie-hypertélorisme oculaire Syndrome de Kapur-Toriello Syndrome de Karsck-Neugebauer Dystrophie musculaire congénitale avec déficience intellectuelle Desmostérolose Syndrome angio-ostéo-hypertrophique Syndrome de Laurin-Sandrow Déficit en pyruvate déshydrogénase E3 Syndrome de macrocéphalie-paraplégie spastique-dysmorphie Syndrome main-pied-utérus Syndrome d'anomalies transverses des membres-hémangiome Syndrome de mésomélie-synostoses Syndactylie type 8 Chondrodysplasie métaphysaire type Spahr Dysplasie spondyloépiphysaire avec raccourcissement des métatarsiens