hypoplasia of the musculature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the musculature. (Human Phenotype Ontology, HP_0009004)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009004
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6 genes associated with the hypoplasia of the musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP6V0A2 ATPase, H+ transporting, lysosomal V0 subunit a2
COLEC11 collectin sub-family member 11
FBN2 fibrillin 2
GLE1 GLE1 RNA export mediator
RBM8A RNA binding motif protein 8A
SALL4 spalt-like transcription factor 4