NM_000414.4(HSD17B4):c.2121+20A>T AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 31, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003809187.1
Allele description
NM_000414.4(HSD17B4):c.2121+20A>T
Condition(s)
- Name:
- Bifunctional peroxisomal enzyme deficiency (DBIF)
- Synonyms:
- D-bifunctional protein deficiency; DBP deficiency; D-bifunctional enzyme deficiency; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009855; MedGen: C0342870; OMIM: 261515
Assertion and evidence details
Last Updated: Mar 5, 2024