Disease #00257 (HNFJ2 (nephropathy, hyperuricemic, familial juvenile, type 2 (HNFJ-2)), OMIM:613092)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HNFJ2
Name	nephropathy, hyperuricemic, familial juvenile, type 2 (HNFJ-2)
OMIM ID	613092
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	REN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-20 21:41:52 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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