SE-ATLAS

Achondrogenesis Achondrogenesis type 1A Achondrogenesis type 1B Achondrogenesis type 2 Achondroplasia Acrocapitofemoral dysplasia Acrodysostosis Acrodysostosis with multiple hormone resistance Acrofacial dysostosis, Catania type Acrofacial dysostosis, Kennedy-Teebi type Acrofacial dysostosis, Palagonia type Acrofacial dysostosis, Rodríguez type Acrofacial dysostosis, Weyers type Acrofrontofacionasal dysostosis Acromesomelic dysplasia, Hunter-Thompson type Acromesomelic dysplasia, Maroteaux type Acromicric dysplasia Albers-Schönberg osteopetrosis Anauxetic dysplasia Aneurysmal bone cyst Astley-Kendall dysplasia Atelosteogenesis type I Atelosteogenesis type II Atelosteogenesis type III Auriculocondylar syndrome Autosomal dominant omodysplasia Autosomal dominant osteopetrosis type 1 Autosomal recessive malignant osteopetrosis Autosomal recessive omodysplasia Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type Baller-Gerold syndrome Blomstrand lethal chondrodysplasia Brachytelephalangic chondrodysplasia punctata Bruck syndrome Camurati-Engelmann disease Cartilage-hair hypoplasia Chondrodysplasia punctata Chondrodysplasia punctata, Toriello type Chondrodysplasia punctata, tibial-metacarpal type Cleidorhizomelic syndrome Cole-Carpenter syndrome Complex lethal osteochondrodysplasia Craniodiaphyseal dysplasia Craniofrontonasal dysplasia Craniolenticulosutural dysplasia Craniometaphyseal dysplasia Craniosynostosis Craniosynostosis, Boston type Craniosynostosis, Philadelphia type Craniosynostosis-dental anomalies Craniosynostosis-intracranial calcifications syndrome Crouzon syndrome Crouzon syndrome-acanthosis nigricans syndrome Desbuquois syndrome Diastrophic dysplasia Dyggve-Melchior-Clausen disease Dysosteosclerosis Dysostosis, Stanescu type Dysplasia of head of femur, Meyer type Dysplastic cortical hyperostosis, Kozlowski-Tsuruta type Dyssegmental dysplasia, Rolland-Desbuquois type Dyssegmental dysplasia, Silverman-Handmaker type Ellis Van Creveld syndrome Endosteal hyperostosis, Worth type Enlarged parietal foramina Familial scaphocephaly syndrome, McGillivray type Fibrochondrogenesis Fibrous dysplasia of bone Frontofacionasal dysplasia Frontorhiny Genochondromatosis type 1 Genochondromatosis type 2 Gnathodiaphyseal dysplasia Greenberg dysplasia Greig cephalopolysyndactyly syndrome Hurler syndrome Hurler-Scheie syndrome Hyaluronidase deficiency Hyperostosis corticalis generalisata Hyperostosis cranialis interna Hypochondrogenesis Hypochondroplasia Hypomandibular faciocranial dysostosis Intermediate osteopetrosis Isolated cloverleaf skull syndrome Isolated osteopoikilosis Isolated oxycephaly Isolated sternocostoclavicular hyperostosis Jeune syndrome Kyphomelic dysplasia Langer mesomelic dysplasia Léri-Weill dyschondrosteosis Maffucci syndrome Mandibulofacial dysostosis Mandibulofacial dysostosis with alopecia Maxillonasal dysplasia Mazabraud syndrome McCune-Albright syndrome Medial condensing osteitis of the clavicle Melorheostosis Mesomelic dwarfism-cleft palate-camptodactyly syndrome Mesomelic dysplasia, Kantaputra type Mesomelic dysplasia, Savarirayan type Metachondromatosis Metaphyseal acroscyphodysplasia Metaphyseal anadysplasia Metaphyseal chondrodysplasia, Jansen type Metaphyseal chondrodysplasia, Kaitila type Metaphyseal chondrodysplasia, Schmid type Metaphyseal chondrodysplasia, Spahr type Metaphyseal dysplasia, Braun-Tinschert type Metatropic dysplasia Monostotic fibrous dysplasia Morgagni-Stewart-Morel syndrome Mucopolysaccharidosis Mucopolysaccharidosis type 1 Mucopolysaccharidosis type 2 Mucopolysaccharidosis type 2, attenuated form Mucopolysaccharidosis type 2, severe form Mucopolysaccharidosis type 3 Mucopolysaccharidosis type 4 Mucopolysaccharidosis type 4A Mucopolysaccharidosis type 4B Mucopolysaccharidosis type 6 Mucopolysaccharidosis type 7 Multiple epiphyseal dysplasia Multiple epiphyseal dysplasia due to collagen 9 anomaly Multiple epiphyseal dysplasia type 1 Multiple epiphyseal dysplasia type 4 Multiple epiphyseal dysplasia type 5 Multiple epiphyseal dysplasia, Al-Gazali type Multiple epiphyseal dysplasia, Beighton type Multiple epiphyseal dysplasia, Lowry type Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia Multiple osteochondromas Multiple synostoses syndrome Nager syndrome Non-syndromic bicoronal craniosynostosis Non-syndromic metopic craniosynostosis Non-syndromic sagittal craniosynostosis Oculomaxillofacial dysostosis Odontochondrodysplasia Ollier disease Omodysplasia Osteogenesis imperfecta Osteogenesis imperfecta type 1 Osteogenesis imperfecta type 2 Osteogenesis imperfecta type 3 Osteogenesis imperfecta type 4 Osteogenesis imperfecta type 5 Osteomesopyknosis Osteopetrosis and related disorders Osteopetrosis with renal tubular acidosis Osteopetrosis-hypogammaglobulinemia syndrome Osteosclerotic metaphyseal dysplasia Otospondylomegaepiphyseal dysplasia Platyspondylic dysplasia, Torrance type Polyostotic fibrous dysplasia Postaxial acrofacial dysostosis Primary basilar invagination Progressive pseudorheumatoid arthropathy of childhood Pseudoachondroplasia Pseudodiastrophic dysplasia Pycnodysostosis Pyknoachondrogenesis Pyle disease Rhizomelic chondrodysplasia punctata Rhizomelic chondrodysplasia punctata type 1 Rhizomelic chondrodysplasia punctata type 2 Rhizomelic chondrodysplasia punctata type 3 Rhizomelic chondrodysplasia punctata type 5 SIX2-related frontonasal dysplasia SPONASTRIME dysplasia Sanfilippo syndrome type A Sanfilippo syndrome type B Sanfilippo syndrome type C Sanfilippo syndrome type D Scheie syndrome Schimke immuno-osseous dysplasia Schneckenbecken dysplasia Schwartz-Jampel syndrome Sclerosteosis Short rib-polydactyly syndrome type 5 Short rib-polydactyly syndrome, Beemer-Langer type Short rib-polydactyly syndrome, Majewski type Short rib-polydactyly syndrome, Saldino-Noonan type Short rib-polydactyly syndrome, Verma-Naumoff type Singleton-Merten dysplasia Smith-McCort dysplasia Solitary bone cyst Spondylocamptodactyly syndrome Spondyloenchondrodysplasia Spondyloepimetaphyseal dysplasia congenita, Strudwick type Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type Spondyloepimetaphyseal dysplasia, Geneviève type Spondyloepimetaphyseal dysplasia, Handigodu type Spondyloepimetaphyseal dysplasia, Irapa type Spondyloepimetaphyseal dysplasia, Missouri type Spondyloepimetaphyseal dysplasia, PAPSS2 type Spondyloepimetaphyseal dysplasia, Shohat type Spondyloepimetaphyseal dysplasia, aggrecan type Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome Spondyloepimetaphyseal dysplasia-hypotrichosis syndrome Spondyloepiphyseal dysplasia congenita Spondyloepiphyseal dysplasia tarda, Kohn type Spondyloepiphyseal dysplasia with metatarsal shortening Spondyloepiphyseal dysplasia, Kimberley type Spondyloepiphyseal dysplasia, MacDermot type Spondyloepiphyseal dysplasia, Maroteaux type Spondyloepiphyseal dysplasia, Reardon type Spondyloepiphyseal dysplasia, Stanescu type Spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome Spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataracts-intellectual disability syndrome Spondylometaphyseal dysplasia, 'corner fracture' type Spondylometaphyseal dysplasia, A4 type Spondylometaphyseal dysplasia, Golden type Spondylometaphyseal dysplasia, Kozlowski type Spondylometaphyseal dysplasia, Schmidt type Spondylometaphyseal dysplasia-cone-rod dystrophy syndrome Stüve-Wiedemann syndrome Summitt syndrome Thanatophoric dysplasia type 1 Thanatophoric dysplasia type 2 Thoracolaryngopelvic dysplasia Treacher-Collins syndrome Upington disease Weismann-Netter syndrome Wildervanck syndrome X-linked calvarial hyperostosis X-linked dominant chondrodysplasia punctata X-linked dominant chondrodysplasia, Chassaing-Lacombe type X-linked mandibulofacial dysostosis X-linked spondyloepimetaphyseal dysplasia