SE-ATLAS

Dysplasie avec gracilité osseuse Dysplasie osseuse primaire condensante Dysplasie osseuse primaire avec hypodensité osseuse Ostéolyse primaire Dysplasie osseuse primaire avec développement anarchique d'un élément du squelette Maladie d'Ollier Syndrome de Maffucci Syndrome d'ostéosclérose-ichtyose-insuffisance ovarienne précoce Rachitisme hypocalcémique Dysplasie campomélique Hyperparathyroïdie primitive sévère néonatale Rachitisme hypophosphatémique Hypercalcémie hypocalciurique familiale type 2 Hypercalcémie hypocalciurique familiale type 1 Dysplasie multi-épiphysaire et pseudoachondroplasie Dysplasie métaphysaire multiple Dysplasie osseuse primaire avec micromélie Dysplasie spondylo-épiphysaire et dysplasie spondylo-épimétaphysaire Dysplasie acromélique Dysplasie mésomélique et rhizo-mésomélique Dysplasie osseuse primaire avec luxations articulaires multiples Hypercalcémie hypocalciurique familiale type 3 Achondroplasie Dysplasie osseuse primaire avec ossification progressive de la peau, des muscles squelettiques, fascias, tendons et ligaments Syndrome de Cole-Carpenter Progéria de Nestor-Guillermo Chondrodysplasie avec luxation articulaire type gPAPP Anadysplasie métaphysaire Syndrome de Roifman Syndrome rhizomélique type Urbach Syndrome de Richieri-Costa-da Silva Gérodermie ostéodysplasique Syndrome de petite taille-onychodysplasie-dysmorphie faciale-hypotrichose Dysplasie spondylo-mégaépiphysaire-métaphysaire Syndrome de Robinow autosomique dominant Dysplasie acromésomélique type Maroteaux Dysplasie mandibulo-acrale avec lipodystrophie de type A Dysplasie mandibulo-acrale avec lipodystrophie de type B Syndrome de Grant Dysplasie acromésomélique type Grebe Ostéopétrose d'Albers-Schönberg Dysplasie dyssegmentaire type Rolland-Desbuquois Dysplasie spondylo-épimétaphysaire type matrilin-3 Syndrome de Hallermann-Streiff Dysplasie de la hanche type Beukes Dysplasie Schneckenbecken Dysostose diaphano-spondylaire Sclérostéose Syndrome de Robinow Syndrome des côtes courtes-polydactylie type Majewski Syndrome des côtes courtes-polydactylie type Beemer-Langer Syndrome des côtes courtes-polydactylie type Verma-Naumoff Syndrome des côtes courtes-polydactylie type Saldino-Noonan Dysplasie thanatophore type 2 Dysplasie fibreuse monostotique Dysplasie fibreuse polyostotique Arthrose précoce avec dysplasie spondyloépiphysaire intermédiaire due à une mutation du gène COL2A1 Dysplasie spondylo-épiphysaire type Kimberley Dysplasie spondylo-épimétaphysaire type PAPPS2 Dysplasie spondylo-épiphysaire tardive Syndrome de Stickler autosomique récessif Syndrome spondylo-camptodactylie Dysplasie épiphysaire multiple due à une anomalie du collagène 9 Hypochondrogenèse Auriculo-ostéodysplasie Brachyolmie type 1 de Hobaek Brachyolmie type 1 de Toledo Brachyolmie type Maroteaux Brachyolmie autosomique dominante Dysplasie épiphysaire multiple type Beighton Dysplasie épiphysaire multiple type 4 Dysplasie épiphysaire multiple type 1 Dysplasie épiphysaire multiple type 5 Hyalinose systémique infantile Dysplasie épiphysaire multiple type Lowry Dysplasie spondylo-métaphysaire type fracture en coins Dysplasie spondylo-métaphysaire type Kozlowski Dysplasie spondylo-métaphysaire type Sedaghatian Syndrome de Stüve-Wiedemann Arthropathie pseudorhumatoïde progressive infantile Dysplasie épiphysaire multiple type Al-Gazali Syndrome CHILD Syndrome de Kenny-Caffey autosomique dominant Syndrome de Kenny-Caffey autosomique récessif Dysplasie épiphysaire multiple avec dysplasie fémorale sévère Omodysplasie autosomique récessive Syndrome de brachydactylie-petite taille-rétinite pigmentaire Omodysplasie autosomique dominante Dysplasie épiphysaire multiple avec miniépiphyse Chondrodysplasie métaphysaire type Kaitila Syndrome tricho-rhino-phalangien Hyperostose de la voûte crânienne liée à l'X Hyperostose corticale dysplasique type Kozlowski-Tsuruta Nanisme microcéphalique primordial Dysplasie spondylo-épimétaphysaire type Strudwick Syndrome Larsen-like de la Réunion Dysplasie spondylo-épimétaphysaire type Irapa Dysplasie spondylo-épimétaphysaire type Shohat Dysplasie SPONASTRIME Dysplasie spondylo-épimétaphysaire avec hyperlaxité ligamentaire Dysplasie platyspondylique type Torrance Syndrome de dysplasie spondylo-épimétaphysaire-membres courts-anomalies de calcification Chondrodysplasie ponctuée rhizomélique Conodysplasie craniofaciale Syndrome d'Alazami Syndrome IMAGe Dysplasie type Astley-Kendall Chérubisme Syndrome de sténose médullaire diaphysaire-tumeur osseuse Dysplasie cranio-métadiaphysaire type os wormien Dysplasie de Singleton-Merten Ostéoporose idiopathique juvénile Ostéolyse expansive familiale Spondylo-oculaire syndrome Syndrome de nodulose-arthropathie-ostéolyse Syndrome de craniosynostose-anomalies anales-porokératose Dysplasie oto-spondylo-mégaépiphysaire autosomique dominante Syndrome d'ostéopétrose-hypogammaglobulinémie Ostéopoecilie isolée Dysplasie en boomerang Syndrome de Dyggve-Melchior-Clausen Ciliopathies avec atteinte osseuse majeure Syndrome d'incurvation congénitale des os longs-petite taille-dolichomacrocéphalie-hypertélorisme oculaire Dysplasie épiphysaire multiple Dysplasie acromésomélique Dysplasie spondylo-métaphysaire Chondrodysplasie ponctuée Dysplasie osseuse primaire par défaut de minéralisation Syndrome d'Ehlers-Danlos spondylodysplasique lié à SLC39A13 Syndrome de Weismann-Netter-Stuhl Chondrodysplasie létale Syndrome de Buschke-Ollendorff Syndrome de Kenny-Caffey Syndrome d'Ellis-Van Creveld Desmostérolose Dysplasie létale Kniest-like Camurati-Engelmann disease Madelung deformity, unilateral Spondyloepimetaphyseal dysplasia, Handigodu type Cheirospondyloenchondromatosis Metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria Larsen-like osseous dysplasia-short stature syndrome Disorders of vitamin D metabolism Hyperostosis corticalis generalisata X-linked dominant chondrodysplasia punctata Phalangeal microgeodic syndrome Hypocalcemic vitamin D-dependent rickets Torg-Winchester syndrome Wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia Lethal chondrodysplasia, Seller type Lethal recessive chondrodysplasia Desbuquois syndrome Familial hypocalciuric hypercalcemia Mandibuloacral dysplasia X-linked skeletal dysplasia-intellectual disability syndrome Cleidorhizomelic syndrome Melnick-Needles syndrome Melorheostosis Mesomelia-synostoses syndrome Upper limb mesomelic dysplasia Metaphyseal dysostosis-intellectual disability-conductive deafness syndrome Ehlers-Danlos/osteogenesis imperfecta syndrome Spondyloepiphyseal dysplasia with metatarsal shortening Anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome Thin ribs-tubular bones-dysmorphism syndrome Coxoauricular syndrome Craniodiaphyseal dysplasia Larsen-like syndrome, B3GAT3 type Chondrodysplasia punctata, Sheffield type Chondrodysplasia punctata, tibial-metacarpal type Larsen syndrome FGFR2-related bent bone dysplasia Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome Spondyloepimetaphyseal dysplasia, Geneviève type Microcephalic primordial dwarfism due to ZNF335 deficiency Dacryocystitis-osteopoikilosis syndrome Stickler syndrome type 1 Stickler syndrome type 2 McCune-Albright syndrome 3M syndrome Geleophysic dysplasia Mesomelic dysplasia, Nievergelt type Metatropic dysplasia Fibular aplasia-complex brachydactyly syndrome Dominant hypophosphatemia with nephrolithiasis or osteoporosis Osteoglosphonic dysplasia Thanatophoric dysplasia Spondylometaphyseal dysplasia, Golden type Axial spondylometaphyseal dysplasia Spondylometaphyseal dysplasia, A4 type Enlarged parietal foramina Talo-patello-scaphoid osteolysis Wolcott-Rallison syndrome Osteogenesis imperfecta Otopalatodigital syndrome Pancreatic insufficiency-anemia-hyperostosis syndrome Omodysplasia Autosomal recessive cutis laxa type 2A Osteocraniostenosis Carpotarsal osteochondromatosis Nasu-Hakola disease Congenital osteogenesis imperfecta-microcephaly-cataracts syndrome Multicentric carpo-tarsal osteolysis with or without nephropathy Severe lateral tibial bowing-short stature-mild winged scapula-mild facial dysmorphism syndrome Osteomesopyknosis Osteopathia striata-cranial sclerosis syndrome Chondroectodermal dysplasia with night blindness Autosomal dominant osteopetrosis type 1 Osteopetrosis with renal tubular acidosis Silver-Russell syndrome due to 7p11.2p13 microduplication Hutchinson-Gilford progeria syndrome Dyschondrosteosis-nephritis syndrome Endosteal hyperostosis, Worth type Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11 Silver-Russell syndrome due to 11p15 microduplication Pseudoachondroplasia Juvenile Paget disease Osteogenesis imperfecta type 4 Osteogenesis imperfecta type 5 OBSOLETE: Peripheral dysostosis Mixed sclerosing bone dystrophy with extra-skeletal manifestations Ghosal hematodiaphyseal dysplasia Rhizomelic dysplasia, Patterson-Lowry type Lowry-Wood syndrome Frontometaphyseal dysplasia Lethal osteosclerotic bone dysplasia Shwachman-Diamond syndrome Silver-Russell syndrome Short stature, Brussels type Stickler syndrome Spondyloperipheral dysplasia-short ulna syndrome Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome Thanatophoric dysplasia type 1 Dyssegmental dysplasia, Silverman-Handmaker type Autosomal dominant hypophosphatemic rickets Brachyolmia-amelogenesis imperfecta syndrome Prenatal benign hypophosphatasia Melorheostosis with osteopoikilosis Infantile hypophosphatasia 12q14 microdeletion syndrome Adult hypophosphatasia Epiphyseal stippling-osteoclastic hyperplasia syndrome Exostoses-anetodermia-brachydactyly type E syndrome Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7 Pyknoachondrogenesis Acromesomelic dysplasia, Hunter-Thompson type Ramon syndrome Acrocapitofemoral dysplasia Intellectual disability-balding-patella luxation-acromicria syndrome Hypocalcemic vitamin D-resistant rickets Anauxetic dysplasia X-linked spondyloepimetaphyseal dysplasia Atelosteogenesis type I X-linked osteoporosis with fractures Severe achondroplasia-developmental delay-acanthosis nigricans syndrome Metaphyseal chondrodysplasia, Schmid type Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome Cartilage-hair hypoplasia Non-rhizomelic chondrodysplasia punctata Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type Smith-McCort dysplasia Mesomelic dysplasia, Savarirayan type Microcephalic osteodysplastic dysplasia, Saul-Wilson type Pseudodiastrophic dysplasia Infantile osteopetrosis with neuroaxonal dysplasia Intermediate osteopetrosis Microcephalic primordial dwarfism, Dauber type Endosteal sclerosis-cerebellar hypoplasia syndrome Metaphyseal dysplasia, Braun-Tinschert type Brachydactyly type A6 Calvarial doughnut lesions-bone fragility syndrome Spondylocarpotarsal synostosis Genochondromatosis type 1 Inclusion body myopathy with Paget disease of bone and frontotemporal dementia Dysspondyloenchondromatosis Genochondromatosis type 2 Metaphyseal acroscyphodysplasia Rare bone disease Autosomal recessive cutis laxa type 2 Léri-Weill dyschondrosteosis Thoracolaryngopelvic dysplasia Fibrous dysplasia of bone Spondylodysplastic dysplasia Campomelic dysplasia and related disorders Neonatal osteosclerotic dysplasia Eiken syndrome Cleidocranial dysplasia and isolated cranial ossification defect Brachyolmia Silver-Russell syndrome due to a point mutation Osteopenia-intellectual disability-sparse hair syndrome Tricho-dento-osseous syndrome Primary hypertrophic osteoarthropathy Caffey disease CHST3-related skeletal dysplasia Campomelia, Cumming type Metaphyseal chondrodysplasia, Jansen type TMEM165-CDG Short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome Madelung deformity, bilateral Dappled diaphyseal dysplasia Spondyloepiphyseal dysplasia, Maroteaux type Multiple osteochondromas Lethal Larsen-like syndrome Upington disease Fibrodysplasia ossificans progressiva Spondyloepimetaphyseal dysplasia, Isidor-Toutain type Spondylometaphyseal dysplasia, Czarny-Ratajczak type Weissenbacher-Zweymuller syndrome Odontochondrodysplasia Lethal chondrodysplasia, Moerman type Chondrodysplasia-difference of sex development syndrome Yunis-Varon syndrome Greenberg dysplasia Otospondylomegaepiphyseal dysplasia Joubert syndrome with Jeune asphyxiating thoracic dystrophy Parietal foramina with clavicular hypoplasia Cleidocranial dysplasia SHOX-related short stature Hypophosphatasia Mazabraud syndrome Gnathodiaphyseal dysplasia Metachondromatosis Metaphyseal chondrodysplasia, Spahr type Metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome Trichorhinophalangeal syndrome type 1 Jeune syndrome Short rib-polydactyly syndrome Autosomal recessive Robinow syndrome Kniest dysplasia Cranioectodermal dysplasia Brachytelephalangic chondrodysplasia punctata Chondrodysplasia punctata, Toriello type Craniometaphyseal dysplasia Cranio-osteoarthropathy Trichorhinophalangeal syndrome type 2 Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome Ear-patella-short stature syndrome Spondyloepimetaphyseal dysplasia, Bieganski type Leukocyte adhesion deficiency type III Ossification anomalies-psychomotor developmental delay syndrome Otopalatodigital syndrome type 1 Otopalatodigital syndrome type 2 Marshall syndrome Terminal osseous dysplasia-pigmentary defects syndrome Brachydactylous dwarfism, Mseleni type Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type Mesomelic dwarfism-cleft palate-camptodactyly syndrome Mesomelic dwarfism, Reinhardt-Pfeiffer type Microcephalic osteodysplastic primordial dwarfism types I and III Microcephalic osteodysplastic primordial dwarfism type II Micromelic dwarfism, Fryns type Microcephalic primordial dwarfism, Toriello type Parastremmatic dwarfism Lenz-Majewski hyperostotic dwarfism Frank-Ter Haar syndrome Spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome Diastrophic dysplasia Lipodystrophy-intellectual disability-deafness syndrome Oculodentodigital dysplasia Autosomal recessive malignant osteopetrosis High bone mass osteogenesis imperfecta Saldino-Mainzer syndrome Dysplasia of head of femur, Meyer type Opsismodysplasia Orofaciodigital syndrome type 4 Progressive osseous heteroplasia Autosomal recessive cutis laxa type 2B Blount disease Bruck syndrome Osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome Autosomal recessive cutis laxa type 2, classic type Autosomal recessive distal osteolysis syndrome Osteopathia striata-pigmentary dermopathy-white forelock syndrome Osteopetrosis and related disorders Osteogenesis imperfecta type 1 Multicentric osteolysis-nodulosis-arthropathy spectrum Osteoporosis-oculocutaneous hypopigmentation syndrome Osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome Osteoporosis-pseudoglioma syndrome Lateral meningocele syndrome Silver-Russell syndrome due to an imprinting defect of 11p15 B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome Pachydermoperiostosis Osteogenesis imperfecta type 3 Dysosteosclerosis Pycnodysostosis Blomstrand lethal chondrodysplasia Dysostosis, Stanescu type Kyphomelic dysplasia Thoracomelic dysplasia Dysplasia epiphysealis hemimelica Schwartz-Jampel syndrome Schimke immuno-osseous dysplasia Seckel syndrome Mesomelic dysplasia, Kantaputra type Ulna metaphyseal dysplasia syndrome Bone dysplasia, lethal Holmgren type Bone dysplasia, Azouz type Spondyloenchondrodysplasia Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome Perinatal lethal hypophosphatasia Spondyloepiphyseal dysplasia, Reardon type X-linked hypophosphatemia Spondyloepiphyseal dysplasia tarda, Kohn type Spondyloepiphyseal dysplasia, MacDermot type Spondyloepimetaphyseal dysplasia, aggrecan type Madelung deformity Spondyloepiphyseal dysplasia congenita Odontohypophosphatasia Achondrogenesis Acrodysostosis Hajdu-Cheney syndrome Pyle disease Acromicric dysplasia Angel-shaped phalango-epiphyseal dysplasia Delayed membranous cranial ossification Fibrochondrogenesis Primary bone dysplasia Atelosteogenesis type II Juvenile hyaline fibromatosis Atelosteogenesis type III Otopalatodigital syndrome spectrum disorder