Disease #01944 (LGMD-2C;SCARMD (dystrophy, muscular, limb-girdle, type 2C (LGMD-2C, severe autosomal recessive muscular dystrophy, North African type (SCARMD))), OMIM:253700)
| Official abbreviation |
LGMD-2C;SCARMD |
| Name |
dystrophy, muscular, limb-girdle, type 2C (LGMD-2C, severe autosomal recessive muscular dystrophy, North African type (SCARMD)) |
| OMIM ID |
253700 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
SGCG |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
