Disease #04288 (LGMDD2;LGMD1F (dystrophy, muscular, limb-girdle, autosomal dominant, type 2 (LGMD1F)), OMIM:608423)
| Official abbreviation |
LGMDD2;LGMD1F |
| Name |
dystrophy, muscular, limb-girdle, autosomal dominant, type 2 (LGMD1F) |
| OMIM ID |
608423 |
| 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 |
TNPO3 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2015-06-19 22:24:12 +02:00 (CEST) |
| Date last edited |
2024-01-12 20:56:41 +01:00 (CET) |
Individuals
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