| Dataset | HPO Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | Aplasia (congenital absence) of the pectoralis minor. (Human Phenotype Ontology, HP_0005255) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0005255 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the absence of pectoralis minor muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| LMX1B | LIM homeobox transcription factor 1, beta |
