Disease #04606 (FSGS7 (glomerulosclerosis, focal segmental, type 7 (FSGS7)), OMIM:616002)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FSGS7
Name	glomerulosclerosis, focal segmental, type 7 (FSGS7)
OMIM ID	616002
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PAX2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:23 +02:00 (CEST)
Date last edited	2020-10-24 17:39:01 +02:00 (CEST)

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