Disease #00241 (WMS2 (Weill-Marchesani syndrome, type 2 (WMS-2)), OMIM:608328)

Official abbreviation WMS2
Name Weill-Marchesani syndrome, type 2 (WMS-2)
OMIM ID 608328
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FBN1
Associated tissues -
Disease features -
Remarks -

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