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Metadata
ID DOID:0110003
Name 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia
Definition A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous mutation in the CLPB gene on chromosome 11q13.
https://www.ncbi.nlm.nih.gov/pubmed/25597510
Xrefs

OMIM:616271

ORDO:445038

Subsets

DO_rare_slim

Synonyms

3-methylglutaconic aciduria type 7 [EXACT]

3-methylglutaconic aciduria type VII [EXACT]

MEGCANN [EXACT]

MGA7 [EXACT]

MGCA7 [EXACT]

Parent Relationships

is_a 3-methylglutaconic aciduria

is_a autosomal recessive disease

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