Disease #03669 (PHA2E (pseudohypoaldosteronism type 2E (PHA2E)), OMIM:614496)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PHA2E
Name	pseudohypoaldosteronism type 2E (PHA2E)
OMIM ID	614496
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CUL3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-08-06 18:44:59 +02:00 (CEST)

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