Disease #02301 (HHT2 (telangiectasia, hemorrhagic, hereditary, type 2 (HHT2)), OMIM:600376)

Official abbreviation HHT2
Name telangiectasia, hemorrhagic, hereditary, type 2 (HHT2)
OMIM ID 600376
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene ACVRL1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-01-11 15:44:29 +01:00 (CET)


Individuals

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00117341 - - - - - Germany - - - - - HHT2 - ACVRL1 ACVRL1 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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