Disease #06727 (LGMDR26 (dystrophy, muscular, limb-girdle, autosomal recessive, type 26), OMIM:618848)
Official abbreviation |
LGMDR26 |
Name |
dystrophy, muscular, limb-girdle, autosomal recessive, type 26 |
OMIM ID |
618848 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
POPDC3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2021-12-10 23:20:41 +01:00 (CET) |
Date last edited |
2024-01-10 22:25:07 +01:00 (CET) |
Individuals
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