RENAL TUBULAR DYSGENESIS Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A developmental defect characterized by absence or poor development of proximal renal tubules. (Human Phenotype Ontology, HP_0008660)
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:267430
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Genes

4 genes/proteins associated with the disease RENAL TUBULAR DYSGENESIS from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
ACE angiotensin I converting enzyme 2.88009
REN renin 2.88009
AGTR1 angiotensin II receptor, type 1 2.88009
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8) 2.88009