NM_000126.4(ETFA):c.201C>G (p.Leu67=) AND Multiple acyl-CoA dehydrogenase deficiency
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001406265.6
Allele description [Variation Report for NM_000126.4(ETFA):c.201C>G (p.Leu67=)]
NM_000126.4(ETFA):c.201C>G (p.Leu67=)
Condition(s)
- Name:
- Multiple acyl-CoA dehydrogenase deficiency (MADD)
- Synonyms:
- GA II; Ethylmalonic-adipicaciduria; Glutaric aciduria, type 2; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009282; MedGen: C0268596; Orphanet: 26791; OMIM: 231680
Assertion and evidence details
Last Updated: Mar 5, 2024