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DO Term : hereditary hemorrhagic telangiectasia [DOID:1270] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A vascular disease characterized by the presence of multiple arteriovenous malformations that lack intervening capillaries and result in direct connections between arteries and veins.

synonyms:
ICD9CM:448.0,
GARD:6626,
ORDO:774,
ICD10CM:I78.0,
OMIM:615506,
NCI:C35064,
SNOMEDCT_US_2023_03_01:266324004,
615506,
OMIM:600376,
UMLS_CUI:C0039445,
Osler-Weber-Rendu disease,
Rendu-Osler-Weber disease,
Osler hemorrhagic telangiectasia syndrome,
MESH:D013683,
187300,
OMIM:187300,
600376

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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