Disease #00254 (RTD (dysgenesis, renal tubular (RTD)), OMIM:267430)

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Official abbreviation	RTD
Name	dysgenesis, renal tubular (RTD)
OMIM ID	267430
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 4 genes	ACE, AGT, AGTR1, REN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-20 21:21:05 +02:00 (CEST)
Date last edited	N/A