Weill-Marchesani syndrome

MONDO:0018096

Weill-Marchesani syndrome (WMS) is a rare condition characterized by short stature, brachydactyly, joint stiffness, and characteristic eye abnormalities including microspherophakia, ectopia of the lens, severe myopia, and glaucoma.

Also known as: Weill Marchesani Syndrome, spherophakia-brachymorphia syndrome, WM syndrome, WMS, mesodermal dysmorphodystrophy congenital

0 clinical trials for this condition and its sub-types, 0 tagged with Weill-Marchesani syndrome itself.

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↑ Syndromic disease (7158) ↑ Autosomal genetic disease (1670) ↑ Multiple congenital anomalies/dysmorphic syndrome without intellectual disability (163) ↑ Acromelic dysplasia (8)

Sub-types of Weill-Marchesani syndrome

Weill-Marchesani 4 syndrome, recessive 0 trials
Weill-Marchesani syndrome 1 0 trials
Weill-Marchesani syndrome 2, dominant 0 trials
Weill-Marchesani syndrome 3 0 trials

Including sub-types (0) Tagged with Weill-Marchesani syndrome (0)

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