Disease #06763 (CMAVM2 (capillary malformation-arteriovenous malformation, type 2), OMIM:618196)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CMAVM2
Name	capillary malformation-arteriovenous malformation, type 2
OMIM ID	618196
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	EPHB4
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2022-03-01 16:56:47 +01:00 (CET)

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