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Weill-Marchesani syndrome 3

rare

Any Weill-Marchesani syndrome in which the cause of the disease is a mutation in the LTBP2 gene.

Identifiers
MONDO:0013899 OMIM:614819
Part of
LTBP2-related ocular dysgenesisWeill-Marchesani syndrome
Also known as
LTBP2 Weill-Marchesani syndrome · Weill-Marchesani syndrome 3, recessive · Weill-Marchesani syndrome caused by mutation in LTBP2 · Weill-Marchesani syndrome type 3 · WMS3

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