Vertigo, benign recurrent, 2

Preferred Label : Vertigo, benign recurrent, 2;

Symbol : BRV2;

CISMeF acronym : BRV2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of benign recurrent vertigo (BRV), see BRV1 (193007).;

Prefixed ID : %613106;

Détails

Origin ID

613106;

UMLS CUI

C2751289;

Currated CISMeF NLP mapping
- vertigo, benign recurrent, 2 [MeSH concept]
- vertigo, benign recurrent, 2 [MeSH Supplementary Concept]
DO Cross reference
- benign paroxysmal positional vertigo [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- vertigo, benign recurrent, 2 [MeSH Supplementary Concept]
- vertigo, benign recurrent, 2 [MeSH concept]

Position du mot-clé dans l'(les) arborescence(s) :

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