Disease #02415 (HCI (hemangioma, capillary infantile (HCI)), OMIM:602089)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	HCI
Name	hemangioma, capillary infantile (HCI)
OMIM ID	602089
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	ANTXR1, FLT4, KDR
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-06-12 11:46:00 +02:00 (CEST)

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