Disease #03907 (LGMDR18;LGMD2S (dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S)), OMIM:615356)
| Official abbreviation |
LGMDR18;LGMD2S |
| Name |
dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S) |
| OMIM ID |
615356 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
5 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TRAPPC11 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-10-24 15:18:22 +02:00 (CEST) |
Individuals
|