Caroli disease

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CAROLI DISEASE
C016251053035MONDO:0010913
IFT56 Causal — Disgenet —
PKHD1 Causal
24710345 26385851
Disgenet, GWAS catalog, Orphanet —
PKD1 Unknown
3178424 9211343 8554072
Disgenet, GenCC
WDR19 Unknown — Disgenet
All4 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Caroli disease.
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autosomal recessive polycystic kidney disease 2 shared genesPKD1, PKHD1 Related via 2 shared genes including PKD1, PKHD1. Liver cyst 1 shared genePKD1 Related via 1 shared gene including PKD1. Congenital hypoplasia of aortic arch 1 shared genePKHD1 Related via 1 shared gene including PKHD1. Periportal fibrosis 1 shared genePKHD1 Related via 1 shared gene including PKHD1. Biliary-renal-neuro-skeletal syndrome 1 shared geneIFT56 Related via 1 shared gene including IFT56.