NM_002529.4(NTRK1):c.2301G>A (p.Glu767=) AND Hereditary insensitivity to pain with anhidrosis
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Dec 2, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001277510.2
Allele description
NM_002529.4(NTRK1):c.2301G>A (p.Glu767=)
Condition(s)
- Name:
- Hereditary insensitivity to pain with anhidrosis (CIPA)
- Synonyms:
- FAMILIAL DYSAUTONOMIA, TYPE II; Insensitivity to pain, congenital, with anhidrosis; Neuropathy, congenital sensory, with anhidrosis; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009746; MedGen: C0020074; Orphanet: 642; OMIM: 256800
Assertion and evidence details
Last Updated: Apr 23, 2022