ATP6V0A2 and Alg9-Congenital Disorder Of Glycosylation: Association Evidence

At a glance

Association overview

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

Provenance

1 source

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

ATP6V0A2

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Alg9-Congenital Disorder Of Glycosylation

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

ClinVar and variant evidence

430 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Literature

11 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Provenance

11 references

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