Disease #01609 (WBS (Williams-Beuren syndrome), OMIM:194050)
| Official abbreviation |
WBS |
| Name |
Williams-Beuren syndrome |
| OMIM ID |
194050 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 2 genes |
ELN, MLXIPL |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2022-02-24 17:26:01 +01:00 (CET) |
Individuals
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