Disease #02436 (DM2 (dystrophy, myotonic, type 2 (DM-2)), OMIM:602668)
| Official abbreviation |
DM2 |
| Name |
dystrophy, myotonic, type 2 (DM-2) |
| OMIM ID |
602668 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
113 |
| Phenotype entries for this disease |
113 |
| Associated with 1 gene |
CNBP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
autosomal dominant |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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