SE-ATLAS

Familial scaphocephaly syndrome, McGillivray type Cole-Carpenter syndrome Achondroplasia Metaphyseal anadysplasia Acrofacial dysostosis, Kennedy-Teebi type Acromesomelic dysplasia, Maroteaux type Albers-Schönberg osteopetrosis Dyssegmental dysplasia, Rolland-Desbuquois type Schneckenbecken dysplasia Crouzon syndrome-acanthosis nigricans syndrome Acrodysostosis with multiple hormone resistance Short rib-polydactyly syndrome, Majewski type Short rib-polydactyly syndrome, Beemer-Langer type Short rib-polydactyly syndrome, Verma-Naumoff type Short rib-polydactyly syndrome, Saldino-Noonan type Thanatophoric dysplasia type 2 Polyostotic fibrous dysplasia Spondyloepiphyseal dysplasia, Kimberley type Spondyloepimetaphyseal dysplasia, PAPSS2 type X-linked mandibulofacial dysostosis Spondylocamptodactyly syndrome Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome Spondyloepimetaphyseal dysplasia, Geneviève type Craniosynostosis, Boston type Rhizomelic chondrodysplasia punctata type 1 Rhizomelic chondrodysplasia punctata type 2 Rhizomelic chondrodysplasia punctata type 3 McCune-Albright syndrome Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type Mesomelic dwarfism-cleft palate-camptodactyly syndrome Metatropic dysplasia Mandibulofacial dysostosis with alopecia Spondylometaphyseal dysplasia, Golden type Spondylometaphyseal dysplasia, A4 type Hypochondrogenesis Multiple epiphyseal dysplasia due to collagen 9 anomaly Achondrogenesis type 2 Achondrogenesis type 1A Achondrogenesis type 1B Multiple epiphyseal dysplasia, Beighton type Multiple epiphyseal dysplasia type 4 Multiple epiphyseal dysplasia type 1 Multiple epiphyseal dysplasia type 5 Spondylometaphyseal dysplasia, 'corner fracture' type Multiple epiphyseal dysplasia, Lowry type 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 Chondrodysplasie ponctuée avec brachytéléphalangie Dysplasie cranio-métaphysaire Chondrodysplasie ponctuée type Toriello Chondrodysplasie ponctuée tibio-métacarpienne Syndrome de dysplasie spondylo-métaphysaire-hypotrichose Craniosynostose Ostéogenèse imparfaite type 1 Ostéogenèse imparfaite type 2 Ostéogenèse imparfaite type 4 Dysostose acrofrontofacionasale Pycnodysostose Dysostose acrofaciale type Palagonia Dysostose acrofaciale type Rodríguez Dysplasie fronto-facio-nasale Chondrodysplasie létale de Blomstrand Dysostose oculo-maxillo-faciale Dysostose type Stanescu Syndrome de Schwartz-Jampel Dysplasie immuno-osseuse de Schimke Dysplasie mésomélique type Kantaputra Syndrome de Maffucci Dysplasie spondylo-enchondrale Acrodysostose Dysostose acrofaciale type Weyers Pycnoachondrogenèse Maladie de Pyle Dysplasie acromésomélique type Hunter-Thompson Dysplasie acromicrique Oxycéphalie isolée Fibrochondrogenèse Atélostéogenèse type II Atélostéogenèse type III Syndrome de Hurler Syndrome de Scheie Syndrome de Hurler-Scheie Hyperostose corticale généralisée Mucopolysaccharidose Syndrome de céphalopolysyndactylie de Greig Maladie de Sanfilippo type A Maladie de Sanfilippo type C Maladie de Sanfilippo type B Maladie de Sanfilippo type D Mélorhéostose Syndrome de Mazabraud Déficit en hyaluronidase Dysplasie cranio-diaphysaire Dysplasie cranio-fronto-nasale Craniosynostose-anomalies dentaires Syndrome de Morgagni-Stewart-Morel Craniosynostose type Philadelphie Kyste osseux solitaire Mucopolysaccharidose type 1 Mucopolysaccharidose type 2 Mucopolysaccharidose type 4 Dysplasie mésomélique type Langer Mucopolysaccharidose type 3 Mucopolysaccharidose type 6 Mucopolysaccharidose type 7 Hyperostose crânienne interne Syndrome de craniosynostose-calcifications intracrâniennes Ostéite condensante médiane de la clavicule Mucopolysaccharidose type 2, forme sévère Chondrodysplasie dominante liée à l'X type Chassaing-Lacombe Syndrome de Summitt Chondrodysplasie métaphysaire type Kaitila Hyperostose corticale dysplasique type Kozlowski-Tsuruta Génochondromatose type 2 Kyste osseux anévrysmal Maladie d'Upington Syndrome de Wildervanck Dysplasie gnatho-diaphysaire Syndrome de Bruck Chondrodysplasie ponctuée rhizomélique type 5 Dysplasie kyphomélique Dysplasie métaphysiaire ostéosclérotique Syndrome des côtes courtes-polydactylie type 5 Dysplasie acro-capito-fémorale Dysplasie frontonasale associée à SIX2