visceral myopathy, familial

Preferred Label : visceral myopathy, familial;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0562874;

UMLS CUI

C0266833;

Currated CISMeF NLP mapping
- Familial visceral myopathy [ICD-11 More detail]
- Familial visceral myopathy [ORDO Disease]
- Hereditary hollow viscus myopathy (disorder) [SNOMED CT concept]
- hereditary hollow viscus myopathy [SNOMED Notion]
Related record
- visceral myopathy, familial [MeSH Supplementary Concept]
See also inter- (CISMeF)
- Visceral myopathy 1 [OMIM Phenotype]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary hollow viscus myopathy (disorder) [SNOMED CT concept]
- hereditary hollow viscus myopathy [SNOMED Notion]