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 Femurkopfdysplasie Typ Meyer Osteomesopyknose Osteopetrose Osteopetrose, autosomal-dominante, Typ 1 Osteopetrose mit renaler tubulärer Azidose Endostale Hyperostose, Typ Worth Pseudoachondroplasie Osteogenesis imperfecta Typ 3 Dysosteosklerose Dysostose, akrofaziale, Catania-Typ Dysostose, faziokraniale hypomandibuläre Osteogenesis imperfecta Typ 5 Dysplasie, spondyloepiphysäre, Typ Nishimura Thanatophore Dysplasie Typ 1 Spondyloepiphysäre Dysplasie-Brachydaktylie-Sprachstörung-Syndrom Dysplasie, dyssegmentale, Typ Silverman-Handmaker Dysplasie, spondyloepiphysäre, Typ Reardon Dysplasie, spondyloepiphysäre, verzögerte, Typ Kohn Dysplasie, spondyloepiphysäre, Typ MacDermot Dysplasie, spondyloepimetaphysäre, Typ Aggrecan Treacher-Collins-Syndrom Dysplasie, spondyloepiphysäre, kongenitaler Typ Achondrogenesie Mukopolysaccharidose Typ 2, attenuierte Form Mukopolysaccharidose Typ 4A Mukopolysaccharidose Typ 4B Sklerosteose Monostotische fibröse Dysplasie Hyperostose, isolierte sternokostoklavikuläre X-chromosomale Hyperostose der Schädelkalotte Binder-Syndrom Primäre basiläre Invagination Dyggve-Melchior-Clausen-Syndrom Léri-Weill-Dyschondrosteose Nager-Syndrom Dysostose, akrofaziale postaxiale Knochendysplasie, fibröse Dysplasie, epiphysäre multiple Chondrodysplasia punctata Weismann-Netter-Syndrom Sagittalnaht-Synostose, nicht-syndromale Synostose, bikoronare, nicht-syndromale Ellis Van Creveld-Syndrom Kraniosynostose, metopische, nicht-syndromale Kleeblattschädel-Syndrom, isoliertes Chondrodysplasie, metaphysäre, Typ Jansen Dysplasie, spondyloepiphysäre, Typ Stanescu Camurati-Engelmann-Syndrom Frontorhinie Dysplasie, spondyloepimetaphysäre, Typ Handigodu Dysplasie, spondyloepiphysäre, Typ Maroteaux Osteochondrome, multiple Metachondromatose Chondrodysplasie, metaphysäre, Typ Spahr Dysplasie, spondyloepiphysäre, mit metatarsaler Verkürzung Jeune-Syndrom Chondrodysplasia punctata, brachytelephalangealer Typ Dysplasie, kranio-metaphysäre Chondrodysplasia punctata Typ Toriello Chondrodysplasia punctata, tibiametakarpaler Typ Spondyloepimetaphysäre Dysplasie-Hypotrichose-Syndrom Kraniosynostose Osteogenesis imperfecta Typ 1 Osteogenesis imperfecta Typ 2 Osteogenesis imperfecta Typ 4 Dysostose, akro-fronto-fazio-nasale Pyknodysostose Dysostose, akrofaziale, Palagonien-Typ Dysostose, akrofaziale, Typ Rodriguez Dysplasie, fronto-fazio-nasale Chondrodysplasie Typ Blomstrand Dysostose, okulo-maxillo-faziale Dysostose Typ Stanescu Schwartz-Jampel-Syndrom Knochendysplasie, immuno-ossäre, Typ Schimke Dysplasie, mesomele, Typ Kantaputra Maffucci-Syndrom Spondyloenchondrodysplasie Akrodysostose Dysostose, akrofaziale, Typ Weyers Pyknoachondrogenesie Pyle-Krankheit Dysplasie, akromesomele, Typ Hunter-Thompson Dysplasie, akromikrische Oxyzephalie, isolierte Fibrochondrogenesie Atelosteogenesis Typ II Atelosteogenesis Typ III Hurler-Syndrom Scheie-Syndrom Hurler-Scheie-Syndrom Hyperostosis corticalis generalisata Mukopolysaccharidose Greig-Zephalopolysyndaktylie-Syndrom Sanfilippo-Krankheit Typ A Sanfilippo-Krankheit Typ C Sanfilippo-Krankheit Typ B Sanfilippo-Krankheit Typ D Melorheostose Mazabraud-Syndrom Hyaluronidasemangel Dysplasie, kraniodiaphysäre Dysplasie, kranio-fronto-nasale Kraniosynostose und Zahnanomalien Stewart-Morel-Morgagni-Syndrom Kraniosynostose Typ Philadelphia Knochenzyste, solitäre Mukopolysaccharidose Typ 1 Mukopolysaccharidose Typ 2 Mukopolysaccharidose Typ 4 Kleinwuchs, mesomeler, Typ Langer Mukopolysaccharidose Typ 3 Mukopolysaccharidose Typ 6 Mukopolysaccharidose Typ 7 Hyperostosis cranialis interna Kraniosynostose-intrakranielle Kalzifizierung-Syndrom Kondensierende Ostitis der medialen Klavikula Mukopolysaccharidose Typ 2, schwere Form Chondrodysplasie, X-chromosomal-dominante, Typ Chassaing-Lacombe Summitt-Syndrom Chondrodysplasie, metaphysäre, Typ Kaitila Dysplastische kortikale Hyperostose Typ Kozlowski-Tsuruta Genochondromatose Typ 2 Aneurysmatische Knochenzyste Upington-Krankheit Wildervanck-Syndrom Dysplasie, gnatho-diaphysäre Bruck-Syndrom Chondrodysplasia punctata, rhizomele, Typ 5 Dysplasie, kyphomele Dysplasie, osteosklerotische metaphysäre Kurzrippen-Polydaktylie-Syndrom Typ 5 Dysplasie, akro-capito-femorale SIX2-assoziierte frontonasale Dysplasie