|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Absence or underdevelopment of the muscles of the upper arm. (Human Phenotype Ontology, HP_0001468)|
|Downloads & Tools|
1 genes associated with the aplasia/hypoplasia involving the musculature of the upper arm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|LMX1B||LIM homeobox transcription factor 1, beta|