Disease #07061 (LGMDR27 (dystrophy, muscular, limb-girdle, autosomal recessive, type 27), OMIM:619566)
| Official abbreviation |
LGMDR27 |
| Name |
dystrophy, muscular, limb-girdle, autosomal recessive, type 27 |
| OMIM ID |
619566 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
JAG2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2024-01-12 21:16:14 +01:00 (CET) |
| Date last edited |
N/A |
Individuals
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