# 3-methylglutaconic aciduria type 1

> 3-methylglutaconic aciduria that has material basis in homozygous or compound heterozygous mutation in the AUH gene on chromosome 9q22

**Wikidata**: [Q27677578](https://www.wikidata.org/wiki/Q27677578)  
**Source**: https://4ort.xyz/entity/3-methylglutaconic-aciduria-type-1


## References

1. Monarch Disease Ontology release 2018-06-29
2. Disease Ontology
3. UniProt
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/681f6747-37ce-498e-8bb1-eddd55a90e2c--2019-03-08T17:00:00)
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/681f6747-37ce-498e-8bb1-eddd55a90e2c--2020-06-29T17:42:31)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_681f6747-37ce-498e-8bb1-eddd55a90e2c-2020-06-29T174231.569Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000148090/MONDO_0009610)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)