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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:3-methylglutaconic aciduria type 7a
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Accession:DOID:0081133 term browser browse the term
Definition:A 3-methylglutaconic aciduria that is characterized primarily by increased levels of 3-methylglutaconic acid (3-MGA) associated with variable neurologic deficits and neutropenia and that has_material_basis_in heterozygous dominant-negative mutation in the CLPB gene on chromosome 11q13. (DO)
Synonyms:exact_synonym: 3-methylglutaconic aciduria type VIIA, autosomal dominant;   3-methylglutaconic aciduria, type VIIA;   MGCA7A
 primary_id: OMIM:619835



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3-methylglutaconic aciduria type 7a term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Clpb ClpB family mitochondrial disaggregase ISO ClinVar Annotator: match by term: 3-METHYLGLUTACONIC ACIDURIA, TYPE VIIA | ClinVar Annotator: match by term: 3-methylglutaconic aciduria, type VIIA OMIM
ClinVar
PMID:25741868 PMID:28492532 PMID:32313153 PMID:34140661 NCBI chr 1:156,028,740...156,158,183
Ensembl chr 1:156,028,930...156,168,788
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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18248
      nervous system disease 14089
        Neurologic Manifestations 10052
          3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia 54
            3-methylglutaconic aciduria type 7a 1
Path 2
Term Annotations click to browse term
  disease 18969
    disease of anatomical entity 18248
      Hemic and Lymphatic Diseases 3849
        hematopoietic system disease 3339
          leukocyte disease 1309
            leukopenia 559
              agranulocytosis 492
                neutropenia 488
                  3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia 54
                    3-methylglutaconic aciduria type 7a 1
paths to the root