Disease #04171 (STRMK (Stormorken syndrome (STRMK)), OMIM:185070)
| Official abbreviation |
STRMK |
| Name |
Stormorken syndrome (STRMK) |
| OMIM ID |
185070 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
STIM1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-01-18 10:53:36 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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