muscular dystrophy, Limb-Girdle, type 2G

Preferred Label : muscular dystrophy, Limb-Girdle, type 2G;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566899;

UMLS CUI

C1866008;

Currated CISMeF NLP mapping
- Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, autosomal recessive 7 [OMIM Phenotype]
- Telethonin-related limb-girdle muscular dystrophy R7 [ORDO Disease]
- autosomal recessive limb-girdle muscular dystrophy type 2G [DO Concept]
- limb girdle muscular dystrophy type 2g [Disease (Nov.)]
Related record
- muscular dystrophy, Limb-Girdle, type 2G [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive limb girdle muscular dystrophy type 2G (disorder) [SNOMED CT concept]
- Muscular dystrophy, limb-girdle, autosomal recessive 7 [OMIM Phenotype]
- Telethonin-related limb-girdle muscular dystrophy R7 [ORDO Disease]