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
|