Disease #03975 (HHT5 (telangiectasia, hemorrhagic, hereditary, type 5 (HHT5)), OMIM:615506)

Global Variome shared LOVD

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Official abbreviation	HHT5
Name	telangiectasia, hemorrhagic, hereditary, type 5 (HHT5)
OMIM ID	615506
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GDF2
Associated tissues	-
Disease features	autosomal dominant
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-11-17 15:31:30 +01:00 (CET)

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