NM_138694.4(PKHD1):c.667+18C>T AND Autosomal recessive polycystic kidney disease
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003822265.2
Allele description [Variation Report for NM_138694.4(PKHD1):c.667+18C>T]
NM_138694.4(PKHD1):c.667+18C>T
Condition(s)
- Name:
- Autosomal recessive polycystic kidney disease (ARPKD)
- Synonyms:
- POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1; POLYCYSTIC KIDNEY DISEASE, INFANTILE, TYPE I; Polycystic kidney disease, infantile type; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009889; MeSH: D017044; MedGen: C0085548; Orphanet: 731; Orphanet: 8378
Assertion and evidence details
Last Updated: Sep 29, 2024