| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Atrophy (wasting) affecting primary type 1 muscle fibers. This feature in general can only be observed on muscle biopsy. (Human Phenotype Ontology, HP_0011807) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0011807 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the type 1 muscle fiber atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| EMD | emerin |
