NM_001113491.2(SEPTIN9):c.*657T>C AND Amyotrophic neuralgia
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000363814.5
Allele description [Variation Report for NM_001113491.2(SEPTIN9):c.*657T>C]
NM_001113491.2(SEPTIN9):c.*657T>C
Condition(s)
- Name:
- Amyotrophic neuralgia
- Synonyms:
- Brachial plexus neuropathy, hereditary; Amyotrophy, hereditary neuralgic, with predilection for brachial plexus; Neuritis with brachial predilection; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008076; MedGen: C1834304; Orphanet: 2901; OMIM: 162100
Assertion and evidence details
Last Updated: Sep 29, 2024