Disease #03599 (EDMD7 (dystrophy, muscular, Emery-Dreifuss, type 7, autosomal dominant (EDMD-7)), OMIM:614302)
| Official abbreviation |
EDMD7 |
| Name |
dystrophy, muscular, Emery-Dreifuss, type 7, autosomal dominant (EDMD-7) |
| OMIM ID |
614302 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
TMEM43 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
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