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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