neuropathy, hereditary sensory, X-Linked

Preferred Label : neuropathy, hereditary sensory, X-Linked;

Origin ID

C564090;

UMLS CUI

C1839602;

Currated CISMeF NLP mapping
- Neuropathy, hereditary sensory, X-linked [OMIM Phenotype]
- hereditary sensory neuropathy X-linked [DO Concept]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- hereditary sensory and autonomic neuropathies [MeSH Descriptor]
Record concept(s)
- neuropathy, hereditary sensory, X-Linked [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Neuropathy, hereditary sensory, X-linked [OMIM Phenotype]
- hereditary sensory neuropathy X-linked [DO Concept]