Cardiomyopathy, familial restrictive, 2

Preferred Label : Cardiomyopathy, familial restrictive, 2;

Symbol : RCM2;

CISMeF acronym : RCM2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of familial restrictive cardiomyopathy, see 115210.;

Prefixed ID : %609578;

Details

Origin ID

609578;

UMLS CUI

C1865071;

Broader ORDO disease(s)
- Familial isolated restrictive cardiomyopathy [ORDO Disease]
Currated CISMeF NLP mapping
- Familial restrictive cardiomyopathy type 2 [ORDO Disease]
- cardiomyopathy, familial restrictive, 2 [MeSH concept]
- cardiomyopathy, familial restrictive, 2 [MeSH Supplementary Concept]
DO Cross reference
- restrictive cardiomyopathy 2 [DO Concept]
ORDO concept(s)
- Familial isolated restrictive cardiomyopathy [ORDO Disease]
- Familial restrictive cardiomyopathy type 2 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial restrictive cardiomyopathy type 2 [ORDO Disease]
- cardiomyopathy, familial restrictive, 2 [MeSH Supplementary Concept]
- cardiomyopathy, familial restrictive, 2 [MeSH concept]
Validated automatic mappings to NTBT
- Familial isolated restrictive cardiomyopathy [ORDO Disease]

Keyword's position in hierarchy(ies) :

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