Rare biliary tract disease

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Rare biliary tract disease

ORPHA:101941Category

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Classified as
Category

Genes reported in subtypes

ABCB4ALG8CEACAM3CEACAM6CFTRCLCA4CYP51A1DCTN4EDNRAGCLCGSTM3HFEHMOX1IL12AIL12RB1IRF5KCNN4LBRLRP5MIFMMEL1PKHD1POU2AF1PRKCSHSEC63SERPINA1SLC11A1SLC26A9SLC6A14SLC9A3SPIBSTX1ATGFB1TNFSF15TNPO3VIPAS39VPS33B

Orphanet records these genes on 8 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

Cross-references

GARD 19791MONDO 15116UMLS C5681785

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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