NM_000303.3(PMM2):c.*275A>T AND PMM2-congenital disorder of glycosylation
- Germline classification:
- Uncertain significance (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:
- RCV000381082.5
Allele description [Variation Report for NM_000303.3(PMM2):c.*275A>T]
NM_000303.3(PMM2):c.*275A>T
Condition(s)
- Name:
- PMM2-congenital disorder of glycosylation
- Synonyms:
- CDG Ia; CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE Ia; CDG 1A; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008907; MedGen: C0349653; Orphanet: 79318; OMIM: 212065
Assertion and evidence details
Last Updated: Sep 1, 2024