dysferlinopathy

Preferred Label : dysferlinopathy;

Origin ID

C537995;

UMLS CUI

C2931687;

Currated CISMeF NLP mapping
- Qualitative or quantitative defects of dysferlin [ORDO Disease]
- dysferlinopathy [Disease (Nov.)]
MeSH term(s) associated for indexing
- muscular dystrophies, limb-girdle [MeSH Descriptor]
Record concept(s)
- Dysferlinopathy [MeSH concept]
See also (suggested by CISMeF)
- limb-girdle muscular dystrophy, type 2B [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Qualitative or quantitative defects of dysferlin [ORDO Disease]
- dysferlinopathy [Disease (Nov.)]