Disease #07069 (BFH2 (hematuria, benign, familial, type 2), OMIM:620320)

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	BFH2
Name	hematuria, benign, familial, type 2
OMIM ID	620320
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	COL4A3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-02-15 12:41:19 +01:00 (CET)
Date last edited	N/A

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