SE-ATLAS

Scaphocéphalie familiale type McGillivray Syndrome de Cole-Carpenter Achondroplasie Anadysplasie métaphysaire Dysostose acrofaciale de Kennedy-Teebi Dysplasie acromésomélique type Maroteaux Ostéopétrose d'Albers-Schönberg Dysplasie dyssegmentaire type Rolland-Desbuquois Dysplasie Schneckenbecken Syndrome de Crouzon-acanthosis nigricans Acrodysostose avec résistance aux multiples hormones 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 polyostotique Dysplasie spondylo-épiphysaire type Kimberley Dysplasie spondylo-épimétaphysaire type PAPPS2 Dysostose mandibulo-faciale liée à l'X Syndrome spondylo-camptodactylie Syndrome de dysplasie spondylo-épimétaphysaire-dentition anormale Dysplasie spondylo-épimétaphysaire type Geneviève Craniosynostose type Boston Chondrodysplasie ponctuée rhizomélique type 1 Chondrodysplasie ponctuée rhizomélique type 2 Chondrodysplasie ponctuée rhizomélique type 3 Syndrome de McCune-Albright Dysplasie spondylo-métaphysaire autosomique récessive type Mégarbané Syndrome de nanisme mésomélique-fente palatine-camptodactylie Dysplasie métatropique Dysostose mandibulo-faciale avec alopécie Dysplasie spondylo-métaphysaire type Golden Dysplasie spondylo-métaphysaire type A4 Hypochondrogenèse Dysplasie épiphysaire multiple due à une anomalie du collagène 9 Achondrogenèse type 2 Achondrogenèse type 1A Achondrogenèse type 1B Dysplasie épiphysaire multiple type Beighton Dysplasie épiphysaire multiple type 4 Dysplasie épiphysaire multiple type 1 Dysplasie épiphysaire multiple type 5 Dysplasie spondylo-métaphysaire type fracture en coins Dysplasie épiphysaire multiple type Lowry Spondylometaphyseal dysplasia, Kozlowski type Spondylometaphyseal dysplasia, Schmidt type Stüve-Wiedemann syndrome Progressive pseudorheumatoid arthropathy of childhood Multiple epiphyseal dysplasia, Al-Gazali type Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia Autosomal recessive omodysplasia Autosomal dominant omodysplasia Anauxetic dysplasia Spondyloepimetaphyseal dysplasia congenita, Strudwick type X-linked spondyloepimetaphyseal dysplasia Multiple synostoses syndrome Atelosteogenesis type I Spondyloepimetaphyseal dysplasia, Irapa type Spondyloepimetaphyseal dysplasia, Shohat type SPONASTRIME dysplasia Spondyloepimetaphyseal dysplasia, Missouri type Metaphyseal chondrodysplasia, Schmid type Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome Cartilage-hair hypoplasia Platyspondylic dysplasia, Torrance type Rhizomelic chondrodysplasia punctata Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type Smith-McCort dysplasia Mesomelic dysplasia, Savarirayan type Astley-Kendall dysplasia Pseudodiastrophic dysplasia Intermediate osteopetrosis Metaphyseal dysplasia, Braun-Tinschert type Singleton-Merten dysplasia Baller-Gerold syndrome Genochondromatosis type 1 Crouzon syndrome Osteopetrosis-hypogammaglobulinemia syndrome Metaphyseal acroscyphodysplasia Isolated osteopoikilosis Thoracolaryngopelvic dysplasia Mandibulofacial dysostosis Ollier disease X-linked dominant chondrodysplasia punctata Odontochondrodysplasia Desbuquois syndrome Greenberg dysplasia Otospondylomegaepiphyseal dysplasia Hypochondroplasia Cleidorhizomelic syndrome Enlarged parietal foramina Diastrophic dysplasia Craniolenticulosutural dysplasia Osteogenesis imperfecta Autosomal recessive malignant osteopetrosis Auriculocondylar syndrome Complex lethal osteochondrodysplasia Omodysplasia Dysplasia of head of femur, Meyer type Osteomesopyknosis Osteopetrosis and related disorders Autosomal dominant osteopetrosis type 1 Osteopetrosis with renal tubular acidosis Endosteal hyperostosis, Worth type Pseudoachondroplasia Osteogenesis imperfecta type 3 Dysosteosclerosis Acrofacial dysostosis, Catania type Hypomandibular faciocranial dysostosis Osteogenesis imperfecta type 5 Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome Thanatophoric dysplasia type 1 Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome Dyssegmental dysplasia, Silverman-Handmaker type Spondyloepiphyseal dysplasia, Reardon type Spondyloepiphyseal dysplasia tarda, Kohn type Spondyloepiphyseal dysplasia, MacDermot type Spondyloepimetaphyseal dysplasia, aggrecan type Treacher-Collins syndrome Spondyloepiphyseal dysplasia congenita Achondrogenesis Mucopolysaccharidosis type 2, attenuated form Mucopolysaccharidosis type 4A Mucopolysaccharidosis type 4B Sclerosteosis Monostotic fibrous dysplasia Isolated sternocostoclavicular hyperostosis X-linked calvarial hyperostosis Maxillonasal dysplasia Primary basilar invagination Dyggve-Melchior-Clausen disease Léri-Weill dyschondrosteosis Nager syndrome Postaxial acrofacial dysostosis Fibrous dysplasia of bone Multiple epiphyseal dysplasia Chondrodysplasia punctata Weismann-Netter syndrome Non-syndromic sagittal craniosynostosis Non-syndromic bicoronal craniosynostosis Ellis Van Creveld syndrome Non-syndromic metopic craniosynostosis Isolated cloverleaf skull syndrome Metaphyseal chondrodysplasia, Jansen type Spondyloepiphyseal dysplasia, Stanescu type Camurati-Engelmann disease Frontorhiny Spondyloepimetaphyseal dysplasia, Handigodu type Spondyloepiphyseal dysplasia, Maroteaux type Multiple osteochondromas Metachondromatosis Metaphyseal chondrodysplasia, Spahr type Spondyloepiphyseal dysplasia with metatarsal shortening Jeune syndrome Brachytelephalangic chondrodysplasia punctata Craniometaphyseal dysplasia Chondrodysplasia punctata, Toriello type Chondrodysplasia punctata, tibial-metacarpal type Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome Craniosynostosis Osteogenesis imperfecta type 1 Osteogenesis imperfecta type 2 Osteogenesis imperfecta type 4 Acrofrontofacionasal dysostosis Pycnodysostosis Acrofacial dysostosis, Palagonia type Acrofacial dysostosis, Rodríguez type Frontofacionasal dysplasia Blomstrand lethal chondrodysplasia Oculomaxillofacial dysostosis Dysostosis, Stanescu type Schwartz-Jampel syndrome Schimke immuno-osseous dysplasia Mesomelic dysplasia, Kantaputra type Maffucci syndrome Spondyloenchondrodysplasia Acrodysostosis Acrofacial dysostosis, Weyers type Pyknoachondrogenesis Pyle disease Acromesomelic dysplasia, Hunter-Thompson type Acromicric dysplasia Isolated oxycephaly Fibrochondrogenesis Atelosteogenesis type II Atelosteogenesis type III Hurler syndrome Scheie syndrome Hurler-Scheie syndrome Hyperostosis corticalis generalisata Mucopolysaccharidosis Greig cephalopolysyndactyly syndrome Sanfilippo syndrome type A Sanfilippo syndrome type C Sanfilippo syndrome type B Sanfilippo syndrome type D Melorheostosis Mazabraud syndrome Hyaluronidase deficiency Craniodiaphyseal dysplasia Craniofrontonasal dysplasia Craniosynostosis-dental anomalies Morgagni-Stewart-Morel syndrome Craniosynostosis, Philadelphia type Solitary bone cyst Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 4 Langer mesomelic dysplasia Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Hyperostosis cranialis interna Craniosynostosis-intracranial calcifications syndrome Medial condensing osteitis of the clavicle Mucopolysaccharidosis type 2, severe form X-linked dominant chondrodysplasia, Chassaing-Lacombe type Summitt syndrome Metaphyseal chondrodysplasia, Kaitila type Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type Genochondromatosis type 2 Aneurysmal bone cyst Upington disease Wildervanck syndrome Gnathodiaphyseal dysplasia Bruck syndrome Rhizomelic chondrodysplasia punctata type 5 Kyphomelic dysplasia Osteosclerotic metaphyseal dysplasia Short rib-polydactyly syndrome type 5 Acrocapitofemoral dysplasia SIX2-related frontonasal dysplasia