Disease #00109 (WDM (myopathy, distal, Welander (WDM)), OMIM:604454)
| Official abbreviation |
WDM |
| Name |
myopathy, distal, Welander (WDM) |
| OMIM ID |
604454 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant, Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TIA1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-01-29 13:42:56 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|