PBC3 and Biliary Cirrhosis, Primary, 3: Association Evidence

Gene-Disorder Association · Article

Gene

PBC3

Biliary Cirrhosis, Primary, 3

Disorder

First reported 1978

Key publication · disorder On the process of cellular division in Escherichia coli: a series of mutants of E. coli altered in the penicillin-binding proteins.Proceedings of the National Academy of Sciences of the United States of America · 1978

Manually curated

Association Review

In brief

The association between PBC3 (Biliary Cirrhosis, Primary, 3) and Biliary Cirrhosis, Primary, 3 is a manually-curated gene–disease association, drawing on a single expert-curated source, which records a susceptibility locus.

Sources 1

Clinical variants 0

Symptoms 0

Compounds 0

Trials 0

Publications 0

At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

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Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

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Biliary Cirrhosis, Primary, 3

The disorder

6 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

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Provenance

References & sources

1 reference

Every source and publication cited across this dossier, as one numbered reference list.

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