Disease association ontology term - MONDO:0013337 - neuropathy, hereditary sensory and autonomic, type 1C
Term summary
- ID
- MONDO:0013337
- Name
- neuropathy, hereditary sensory and autonomic, type 1C
- Ontology or CV name
- Disease association
- Definition
- A hereditary sensory and autonomic neuropathy type 1 that has material basis in heterozygous mutation in the SPTLC2 gene on chromosome 14q24.
