aplasia of the abdominal wall musculature Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the abdominal musculature. (Human Phenotype Ontology, HP_0005199)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005199
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Genes

1 genes associated with the aplasia of the abdominal wall musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CHRM3 cholinergic receptor, muscarinic 3