Disease #05806 (RHDA3 (hypodysplasia/aplasia, renal, type 3 (RHDA-3), OMIM:617805)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	RHDA3
Name	hypodysplasia/aplasia, renal, type 3 (RHDA-3
OMIM ID	617805
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GREB1L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-07 10:00:28 +02:00 (CEST)
Date last edited	N/A

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