Absent tibia - polydactyly - arachnoid cyst
|
(Orphanet:3328)
|
Acromesomelic dysplasia, Hunter-Thomson type
|
(Orphanet:968)
|
Acromesomelic dysplasia, Maroteaux type
|
(Orphanet:40)
|
Atelosteogenesis type I
|
(Orphanet:1190)
|
Atelosteogenesis type III
|
(Orphanet:56305)
|
Dyschondrosteosis - nephritis
|
(Orphanet:1765)
|
Fuhrmann syndrome
|
(Orphanet:2854)
|
HYPOPROTEINEMIA, HYPERCATABOLIC
|
(OMIM:241600)
|
Kyphomelic dysplasia
|
(Orphanet:1801)
|
Langer mesomelic dysplasia
|
(Orphanet:2632)
|
Léri-Weill dyschondrosteosis
|
(Orphanet:240)
|
MESOMELIC DYSPLASIA, KANTAPUTRA TYPE
|
(OMIM:156232)
|
Marshall syndrome
|
(Orphanet:560)
|
Mesomelic dysplasia, Kantaputra type
|
(Orphanet:1836)
|
Metaphyseal anadysplasia
|
(Orphanet:1040)
|
Microcephalic osteodysplastic primordial dwarfism type 2
|
(Orphanet:2637)
|
OSTEOGENESIS IMPERFECTA, TYPE VIII
|
(OMIM:610915)
|
Ophthalmomandibulomelic dysplasia
|
(Orphanet:2741)
|
Otopalatodigital syndrome
|
(Orphanet:669)
|
Otopalatodigital syndrome type 2
|
(Orphanet:90652)
|
Phocomelia, Schinzel type
|
(Orphanet:2879)
|
Postaxial tetramelic oligodactyly
|
(Orphanet:2730)
|
Radio-ulnar synostosis - amegakaryocytic thrombocytopenia
|
(Orphanet:71289)
|
Spondyloepimetaphyseal dysplasia with joint laxity
|
(Orphanet:93359)
|
Spondyloepimetaphyseal dysplasia, Missouri type
|
(Orphanet:93356)
|
Upper limb mesomelic dysplasia
|
(Orphanet:2497)
|
W syndrome
|
(Orphanet:2804)
|