3-methylglutaconic aciduria, type viia

Preferred Label : 3-methylglutaconic aciduria, type viia;

Symbol : MGCA7A;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : 3-methylglutaconic aciduria with neurologic involvement and neutropenia, autosomal dominant;

Prefixed ID : #619835;

Details

Origin ID

619835;

UMLS CUI

C5676967;

Genes related to phenotype
- Caseinolytic peptidase b [OMIM gene]
ORDO concept(s)
- 3-methylglutaconic aciduria type 7 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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