Achondroplasia
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(Orphanet:15)
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Acrocapitofemoral dysplasia
|
(Orphanet:63446)
|
Autosomal dominant brachyolmia
|
(Orphanet:93304)
|
Axial spondylometaphyseal dysplasia
|
(Orphanet:168549)
|
BARATELA-SCOTT SYNDROME
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(OMIM:300881)
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Brachyolmia
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(Orphanet:1293)
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Brachyolmia type 1, Hobaek type
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(Orphanet:93301)
|
Brachyolmia type 1, Toledo type
|
(Orphanet:93303)
|
CHONDRODYSPLASIA, ACROMESOMELIC, WITH GENITAL ANOMALIES
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(OMIM:609441)
|
CHST3-related skeletal dysplasia
|
(Orphanet:263463)
|
Camptodactyly syndrome, Guadalajara type 1
|
(Orphanet:1327)
|
Cleidocranial dysplasia
|
(Orphanet:1452)
|
Coats plus syndrome
|
(Orphanet:313838)
|
Czech dysplasia, metatarsal type
|
(Orphanet:137678)
|
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED
|
(OMIM:304950)
|
Desbuquois syndrome
|
(Orphanet:1425)
|
Ehlers-Danlos syndrome, spondylocheirodysplastic type
|
(Orphanet:157965)
|
Langer mesomelic dysplasia
|
(Orphanet:2632)
|
Lipodystrophy - intellectual deficit - deafness
|
(Orphanet:50811)
|
METAPHYSEAL ANADYSPLASIA 2
|
(OMIM:613073)
|
Multiple epiphyseal dysplasia type 1
|
(Orphanet:93308)
|
Multiple epiphyseal dysplasia type 5
|
(Orphanet:93311)
|
Multiple epiphyseal dysplasia, Lowry type
|
(Orphanet:166016)
|
Multiple epiphyseal dysplasia, with miniepiphyses
|
(Orphanet:166032)
|
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia
|
(Orphanet:166029)
|
RHIZOMELIC DYSPLASIA, SCOLIOSIS, AND RETINITIS PIGMENTOSA
|
(OMIM:610319)
|
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED
|
(OMIM:313400)
|
Saldino-Mainzer syndrome
|
(Orphanet:140969)
|
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome
|
(Orphanet:314394)
|
Spondyloepimetaphyseal dysplasia - abnormal dentition
|
(Orphanet:168451)
|
Spondyloepimetaphyseal dysplasia - hypotrichosis
|
(Orphanet:168443)
|
Spondyloepimetaphyseal dysplasia with joint laxity
|
(Orphanet:93359)
|
Spondyloepimetaphyseal dysplasia, Bieganski type
|
(Orphanet:168448)
|
Spondyloepimetaphyseal dysplasia, Geneviève type
|
(Orphanet:168454)
|
Spondyloepimetaphyseal dysplasia, Shohat type
|
(Orphanet:93352)
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
(Orphanet:93315)
|