cervical hypertrichosis neuropathy

Preferred Label : cervical hypertrichosis neuropathy;

MeSH note : Familial congenital anterior cervical hypertrichosis associated with peripheral sensory and motor neuropathy; Hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy;

Details

Origin ID

C537956;

UMLS CUI

C2931676;

Automatic exact mappings (from CISMeF team)
- Cervical hypertrichosis-peripheral neuropathy syndrome [ORDO Disease]
- Hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy [OMIM Phenotype]
MeSH term(s) associated for indexing
- cervix uteri [MeSH Descriptor]
- hereditary sensory and autonomic neuropathies [MeSH Descriptor]
- hypertrichosis [MeSH Descriptor]
Record concept(s)
- Cervical hypertrichosis neuropathy [MeSH concept]
See also inter- (CISMeF)
- Cervical hypertrichosis and peripheral neuropathy syndrome (disorder) [SNOMED CT concept]
- Cervical hypertrichosis-peripheral neuropathy syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cervical hypertrichosis-peripheral neuropathy syndrome [ORDO Disease]

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