neuropathy, hereditary thermosensitive

Preferred Label : neuropathy, hereditary thermosensitive;

Origin ID

C566575;

UMLS CUI

C1865856;

Automatic exact mappings (from CISMeF team)
- Hereditary thermosensitive neuropathy [ICD-11 More detail]
CISMeF manual mappings
- Hereditary thermosensitive neuropathy (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hereditary thermosensitive neuropathy [ORDO Disease]
- Neuropathy, hereditary thermosensitive [OMIM Phenotype]
MeSH term(s) associated for indexing
- hereditary sensory and motor neuropathy [MeSH Descriptor]
Record concept(s)
- neuropathy, hereditary thermosensitive [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary thermosensitive neuropathy [ORDO Disease]
- Hereditary thermosensitive neuropathy (disorder) [SNOMED CT concept]
- Neuropathy, hereditary thermosensitive [OMIM Phenotype]