Disease #05697 (BARTS5 (Bartter syndrome, type 5, antenatal, transient (BARTS5)), OMIM:300971)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	BARTS5
Name	Bartter syndrome, type 5, antenatal, transient (BARTS5)
OMIM ID	300971
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MAGED2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-17 16:55:00 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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