aplasia/hypoplasia involving the shoulder musculature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the muscles of the shoulder. (Human Phenotype Ontology, HP_0001464)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001464
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Genes

2 genes associated with the aplasia/hypoplasia involving the shoulder musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
RBM8A RNA binding motif protein 8A
SALL4 spalt-like transcription factor 4