# 3-methylglutaconic aciduria type 5

> 3-methylglutaconic aciduria that has material basis in homozygous mutation in the DNAJC19 gene on chromosome 3q26

**Wikidata**: [Q24960528](https://www.wikidata.org/wiki/Q24960528)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Dilated_cardiomyopathy_with_ataxia_syndrome)  
**Source**: https://4ort.xyz/entity/3-methylglutaconic-aciduria-type-5


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. Mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_fa7f8087-632d-4044-9e20-722085c3b42c-2021-09-24T024347.391Z)
6. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000205981/MONDO_0012435)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000205981/Orphanet_66634)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)