Tomaculous neuropathy

Preferred Label : Tomaculous neuropathy;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0531426;

UMLS CUI

C0393814;

Automatic exact mappings (from CISMeF team)
- Hereditary neuropathy with liability to pressure palsies [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hereditary liability to pressure palsies (disorder) [SNOMED CT concept]
- Hereditary neuropathy with liability to pressure palsies [MedDRA Preferred Term]
- Hereditary neuropathy with liability to pressure palsies [ORDO Disease]
- Neuropathy, hereditary, with liability to pressure palsies [OMIM Phenotype]
- Tomaculous neuropathy [MedDRA LLT]
- Tomaculous neuropathy [PASCAL descriptor]
- hereditary neuropathy with liability to pressure palsies [Disease (Nov.)]
- hereditary neuropathy with liability to pressure palsies [DO Concept]
Related record
- tomaculous neuropathy [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary liability to pressure palsies (disorder) [SNOMED CT concept]
- Hereditary neuropathy with liability to pressure palsies [MedDRA Preferred Term]
- Hereditary neuropathy with liability to pressure palsies [ORDO Disease]
- Neuropathy, hereditary, with liability to pressure palsies [OMIM Phenotype]
- Tomaculous neuropathy [MedDRA LLT]
- hereditary neuropathy with liability to pressure palsies [DO Concept]
- hereditary neuropathy with liability to pressure palsies [Disease (Nov.)]