Genopathy
Gene-Disorder Association · Article
Gene
MMACHC
Metabolism Of Cobalamin Associated C
Manually curatedApproved treatment annotated
Association Review

In brief

The association between MMACHC (Metabolism Of Cobalamin Associated C) and Vitamin B12 Deficiency is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 2
Trials 11of 78 via MMACHC compounds
Publications 0
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
MMACHC

The gene

1 source summary

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

Request access
04
Vitamin B12 Deficiency

The disorder

4 database identifiers

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

Request access
05
Mechanism overlap

Shared mechanisms

2 shared pathways

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
06
Interventions

Therapeutics

2 compounds & drugs

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

Request access
07
Human studies

Clinical trials

78 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

Request access
08
Provenance

References & sources

9 references

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

Request access