NM_024079.5(ALG8):c.1276+10G>A AND ALG8 congenital disorder of glycosylation
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 19, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001520139.13
Allele description [Variation Report for NM_024079.5(ALG8):c.1276+10G>A]
NM_024079.5(ALG8):c.1276+10G>A
Condition(s)
- Name:
- ALG8 congenital disorder of glycosylation
- Synonyms:
- CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ih; CDG Ih; Congenital disorder of glycosylation type 1H; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0011969; MedGen: C2931002; Orphanet: 79325; OMIM: 608104
Assertion and evidence details
Last Updated: Jun 2, 2024