SEC61B-related polycystic liver disease
MONDO:0550003Mondo
Findings
No curated finding names SEC61B-related polycystic liver disease yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any autosomal dominant polycystic liver disease in which the cause of the disease is a mutation in the SEC61B gene.
Definition from the Mondo Disease Ontology (MONDO:0550003), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- SEC61BHGNC:16993
- Limited · ClinGen · Autosomal dominant · 2023