Disease #02405 (LGMDR7;LGMD2G (dystrophy, muscular, limb-girdle, type 2G), OMIM:601954)
| Official abbreviation |
LGMDR7;LGMD2G |
| Name |
dystrophy, muscular, limb-girdle, type 2G |
| OMIM ID |
601954 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 1 gene |
TCAP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2023-01-19 16:08:09 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|