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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 3
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Accession:DOID:0110004 term browser browse the term
Definition:A 3-methylglutaconic aciduria that has_material_basis_in mutation in the OPA3 gene. (DO)
Synonyms:exact_synonym: 3-methylglutaconic aciduria, type III;   Costeff optic atrophy syndrome;   Costeff syndrome;   Iraqi Jewish optic atrophy plus;   MGA, type III;   MGA3;   MGCA3;   OPA3, Autosomal Recessive;   Optic Atrophy 3, Autosomal Recessive;   autosomal recessive optic atrophy plus syndrome;   autosomal recessive optic atrophy type 3;   infantile optic atrophy with chorea and spastic paraplegia;   optic atrophy plus syndrome
 primary_id: MESH:C535311
 alt_id: OMIM:258501
 xref: ORDO:67047


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3-methylglutaconic aciduria type 3 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G DNAJC19 DnaJ heat shock protein family (Hsp40) member C19 ISO ClinVar Annotator: match by term: 3-Methylglutaconic aciduria type 3 ClinVar PMID:16055927 PMID:27928778 PMID:28492532 NCBI chr 3:178,019,161...178,025,272
Ensembl chr 3:186,191,128...186,195,666 		JBrowse link
G OPA3 outer mitochondrial membrane lipid metabolism regulator OPA3 ISO ClinVar Annotator: match by term: 3-Methylglutaconic aciduria type 3 | ClinVar Annotator: match by term: Costeff optic atrophy syndrome OMIM
ClinVar		 PMID:9536098 PMID:11668429 PMID:12126933 PMID:15342707 PMID:15902555 More... NCBI chr19:42,477,467...42,546,814
Ensembl chr19:51,073,322...51,130,555 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17996
    Nutritional and Metabolic Diseases 7184
      disease of metabolism 7184
        inherited metabolic disorder 5521
          3-methylglutaconic aciduria 160
            3-methylglutaconic aciduria type 3 2
Path 2
Term Annotations click to browse term
  disease 17996
    disease of anatomical entity 15260
      nervous system disease 13293
        central nervous system disease 11923
          brain disease 11204
            movement disease 2498
              Dyskinesias 2132
                choreatic disease 446
                  3-methylglutaconic aciduria type 3 2
paths to the root