Disease #00090 (WMS2 (WEILL-MARCHESANI SYNDROME 2), OMIM:608328)

Official abbreviation WMS2
Name WEILL-MARCHESANI SYNDROME 2
OMIM ID 608328
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene FBN1
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:15:51 +00:00 (UTC)
Date last edited N/A

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