3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria that has material basis in homozygous mutation in the DNAJC19 gene on chromosome 3q26
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3-methylglutaconic aciduria type 5
Summary
3-methylglutaconic aciduria type 5 is a rare disease[1]. It is known by 18 alternative names across languages and contexts.[2]
Key Facts
- 3-methylglutaconic aciduria type 5's instance of is recorded as rare disease[3].
- 3-methylglutaconic aciduria type 5's instance of is recorded as class of disease[4].
- 3-methylglutaconic aciduria type 5 is a type of 3-methylglutaconic aciduria[5].
- 3-methylglutaconic aciduria type 5 is a type of syndrome associated with dilated cardiomyopathy[6].
- 3-methylglutaconic aciduria type 5 is a type of genetic disease[7].
- 3-methylglutaconic aciduria type 5 is a type of autosomal recessive disease[8].
- 3-methylglutaconic aciduria type 5's NCI Thesaurus ID is recorded as C173146[9].
- 3-methylglutaconic aciduria type 5's health specialty is recorded as medical genetics[10].
- 3-methylglutaconic aciduria type 5's health specialty is recorded as cardiology[11].
- 3-methylglutaconic aciduria type 5's health specialty is recorded as pediatrician[12].
- 3-methylglutaconic aciduria type 5's genetic association is recorded as DNAJC19[13].
- 3-methylglutaconic aciduria type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110000[14].
- 3-methylglutaconic aciduria type 5's exact match is recorded as http://identifiers.org/doid/DOID:0110000[15].
- 3-methylglutaconic aciduria type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
3-methylglutaconic aciduria type 5 is known by 18 alternative names across languages and contexts.[2]