aplasia/hypoplasia of the bladder Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the urinary bladder. (Human Phenotype Ontology, HP_0010476)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010476
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Genes

1 genes associated with the aplasia/hypoplasia of the bladder phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MKS1 Meckel syndrome, type 1