renal tubular dysgenesis Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect characterized by absence or poor development of proximal renal tubules. (Human Phenotype Ontology, HP_0008660)
External Link http://www.omim.org/entry/267430
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Genes

4 genes associated with the renal tubular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
REN renin