Limb-girdle muscular dystrophy, type 2B

Preferred Label : Limb-girdle muscular dystrophy, type 2B;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0530360;

UMLS CUI

C1850889;

Currated CISMeF NLP mapping
- Autosomal recessive limb girdle muscular dystrophy type 2B (disorder) [SNOMED CT concept]
- Dysferlin-related limb-girdle muscular dystrophy R2 [ORDO Disease]
- Limb-Girdle Muscular Dystrophy Type 2B [NCIt concept]
- Muscular dystrophy, limb-girdle, autosomal recessive 2 [OMIM Phenotype]
- autosomal recessive limb-girdle muscular dystrophy type 2B [DO Concept]
- limb girdle muscular dystrophy type 2b [Disease (Nov.)]
Related record
- limb-girdle muscular dystrophy, type 2B [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive limb girdle muscular dystrophy type 2B (disorder) [SNOMED CT concept]
- Dysferlin-related limb-girdle muscular dystrophy R2 [ORDO Disease]
- Limb-Girdle Muscular Dystrophy Type 2B [NCIt concept]
- Muscular dystrophy, limb-girdle, autosomal recessive 2 [OMIM Phenotype]