Disease #05656 (LGMDD4;LGMD1I (dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I)), OMIM:618129)
Official abbreviation |
LGMDD4;LGMD1I |
Name |
dystrophy, muscular, limb-girdle, autosomal dominant, type 4 (LGMDD-4, LGMD-1I) |
OMIM ID |
618129 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
CAPN3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
autosomal dominant |
Date created |
2019-09-16 23:11:06 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|