Telangiectasia, hereditary hemorrhagic, type 3

Preferred Label : Telangiectasia, hereditary hemorrhagic, type 3;

Obsolete resource : true;

Moved to : 187300;

Symbol : HHT3;

CISMeF acronym : HHT3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of HHT, see 187300.;

Prefixed ID : 601101;

Details

Origin ID

601101;

UMLS CUI

C1832774;

DO Cross reference
- hereditary hemorrhagic telangiectasia [DO Concept]
ORDO concept(s)
- Hereditary hemorrhagic telangiectasia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Osler-rendu-weber syndrome 3 [MeSH concept]
- osler-rendu-weber syndrome 3 [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- Hereditary hemorrhagic telangiectasia [ORDO Disease]

Keyword's position in hierarchy(ies) :

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