Adams-Oliver syndrome
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(Orphanet:974)
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Arthrogryposis multiplex congenita
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(Orphanet:1037)
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Autosomal recessive amelia
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(Orphanet:1027)
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Cutis marmorata telangiectatica congenita
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(Orphanet:1556)
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Distal monosomy 17q
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(Orphanet:1597)
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Dysplastic cortical hyperostosis
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(Orphanet:2204)
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Fibulo-ulnar hypoplasia - renal anomalies
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(Orphanet:2256)
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Hutchinson-Gilford progeria syndrome
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(Orphanet:740)
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Hypotrichosis with juvenile macular degeneration
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(Orphanet:1573)
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Lipodystrophy due to peptidic growth factors deficiency
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(Orphanet:1979)
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Madelung deformity
|
(Orphanet:35688)
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Neu-Laxova syndrome
|
(Orphanet:2671)
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Neurogenic arthrogryposis multiplex congenita
|
(Orphanet:1143)
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Odontotrichomelic syndrome
|
(Orphanet:2723)
|
Parkes Weber syndrome
|
(Orphanet:90307)
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Trisomy 18
|
(Orphanet:3380)
|