1p36 deletion syndrome
|
(Orphanet:1606)
|
Atelosteogenesis type I
|
(Orphanet:1190)
|
Blackfan-Diamond anemia
|
(Orphanet:124)
|
CAMPOMELIC DYSPLASIA
|
(OMIM:114290)
|
Campomelic dysplasia
|
(Orphanet:140)
|
Cerebro-costo-mandibular syndrome
|
(Orphanet:1393)
|
Cloacal exstrophy
|
(Orphanet:93929)
|
DIAMOND-BLACKFAN ANEMIA 1
|
(OMIM:105650)
|
Exstrophy-epispadias complex
|
(Orphanet:322)
|
Greenberg dysplasia
|
(Orphanet:1426)
|
Holoprosencephaly - postaxial polydactyly
|
(Orphanet:2166)
|
Intellectual deficit, X-linked - dysmorphism - cerebral atrophy
|
(Orphanet:2958)
|
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
|
(OMIM:210710)
|
Microcephalic osteodysplastic primordial dwarfism types 1 and 3
|
(Orphanet:2636)
|
SECKEL SYNDROME 1
|
(OMIM:210600)
|
Seckel syndrome
|
(Orphanet:808)
|
Spondyloepimetaphyseal dysplasia with joint laxity
|
(Orphanet:93359)
|
Spondylometaphyseal dysplasia, Sedaghatian type
|
(Orphanet:93317)
|
X-linked dominant chondrodysplasia, Chassaing-Lacombe type
|
(Orphanet:163966)
|