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DO Term : 3-methylglutaconic aciduria type 7b [DOID:0081134] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A 3-methylglutaconic aciduria that has_material_basis_in homozygous or compound heterozygous loss-of-function mutations in the CLPB gene on chromosome 11q13.
  • synonyms:
  • OMIM:616271,
  • 616271
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents