Disease #00168 (WMS; WS (Williams-Beuren syndrome), OMIM:194050)
Official abbreviation |
WMS; WS |
Name |
Williams-Beuren syndrome |
OMIM ID |
194050 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
NCF1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2023-01-04 17:49:08 +08:00 (CST) |
Date last edited |
N/A |
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