Disease #00419 (MWKS (Marden Walker syndrome (MWKS)), OMIM:248700)
| Official abbreviation |
MWKS |
| Name |
Marden Walker syndrome (MWKS) |
| OMIM ID |
248700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PIEZO2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-06-16 13:07:26 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|