Miyoshi muscular dystrophy 2

Preferred Label : Miyoshi muscular dystrophy 2;

Symbol : MMD2;

CISMeF acronym : MMD2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Miyoshi myopathy 2;

Description : For a general phenotypic description and a discussion of genetic heterogeneity of Miyoshi muscular dystrophy, see MMD1 (254130).;

Prefixed ID : %613318;

Details

Origin ID

613318;

UMLS CUI

C2750077;

Automatic exact mappings (from CISMeF team)
- Miyoshi muscular dystrophy 2 [DO Concept]
- monocyte to macrophage differentiation associated 2 [HGNC gene]
Currated CISMeF NLP mapping
- miyoshi muscular dystrophy 2 [MeSH concept]
- miyoshi muscular dystrophy 2 [MeSH Supplementary Concept]
DO Cross reference
- Miyoshi muscular dystrophy 2 [DO Concept]
ORDO concept(s)
- Miyoshi myopathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- miyoshi muscular dystrophy 2 [MeSH Supplementary Concept]
- miyoshi muscular dystrophy 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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