Achondrogenesis type 1B
|
(Orphanet:93298)
|
Anauxetic dysplasia
|
(Orphanet:93347)
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Blackfan-Diamond anemia
|
(Orphanet:124)
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DIAMOND-BLACKFAN ANEMIA 1
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(OMIM:105650)
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FIBROCHONDROGENESIS 2
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(OMIM:614524)
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Hurler syndrome
|
(Orphanet:93473)
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Lethal Kniest-like dysplasia
|
(Orphanet:2347)
|
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I
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(OMIM:210710)
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Marshall syndrome
|
(Orphanet:560)
|
Metaphyseal chondrodysplasia, Kaitila type
|
(Orphanet:166038)
|
Microcephalic osteodysplastic primordial dwarfism types 1 and 3
|
(Orphanet:2636)
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Otopalatodigital syndrome
|
(Orphanet:669)
|
Otopalatodigital syndrome type 2
|
(Orphanet:90652)
|
Pelvis-shoulder dysplasia
|
(Orphanet:2839)
|
Pelviscapular dysplasia
|
(Orphanet:93333)
|
Platyspondylic dysplasia, Torrance type
|
(Orphanet:85166)
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Severe achondroplasia - developmental delay - acanthosis nigricans
|
(Orphanet:85165)
|
Spondylo-megaepiphyseal-metaphyseal dysplasia
|
(Orphanet:228387)
|
THANATOPHORIC DYSPLASIA, TYPE II
|
(OMIM:187601)
|
Thanatophoric dysplasia type 1
|
(Orphanet:1860)
|
Wiedemann-Rautenstrauch syndrome
|
(Orphanet:3455)
|