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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:nuclear type mitochondrial complex I deficiency 20
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Accession:DOID:0112072 term browser browse the term
Definition:A nuclear type mitochondrial complex I deficiency characterized by infantile onset of acute metabolic acidosis, hypertrophic cardiomyopathy, and muscle weakness associated with deficiency of mitochondrial complex I activity in muscle, liver, and fibroblasts that has_material_basis_in homozygous or compound heterozygous mutation in ACAD9 on chromosome 3q21.3. (DO)
Synonyms:exact_synonym: ACAD9 deficiency;   ACYL-CoA DEHYDROGENASE 9 DEFICIENCY;   MC1DN20;   deficiency of acyl-CoA dehydrogenase family, member 9;   mitochondrial complex 1 deficiency due to ACAD9 deficiency;   mitochondrial complex I deficiency due to ACAD9 deficiency
 primary_id: MESH:C567006
 alt_id: OMIM:611126
 xref: ORDO:99901
For additional species annotation, visit the Alliance of Genome Resources.


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nuclear type mitochondrial complex I deficiency 20 term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Acad9 acyl-CoA dehydrogenase family, member 9 ISO ClinVar Annotator: match by term: Acyl-CoA dehydrogenase family, member 9, deficiency of
CTD Direct Evidence: marker/mechanism
ClinVar Annotator: match by OMIM:611126
OMIM
ClinVar
CTD
PMID:7599230 PMID:17564966 PMID:20816094 PMID:20929961 PMID:21057504 PMID:22200994 PMID:22277967 PMID:22499348 PMID:25326637 PMID:25721401 PMID:25741868 PMID:26669660 PMID:27233227 PMID:27290639 PMID:27884173 PMID:28279569 PMID:28492532 PMID:28529009 PMID:30025539 PMID:30311383 PMID:32313153 NCBI chr 2:122,782,051...122,806,166
Ensembl chr 2:122,782,060...122,805,768
JBrowse link
G Cfap92 cilia and flagella associated protein 92 ISO ClinVar Annotator: match by term: Acyl-CoA dehydrogenase family, member 9, deficiency of ClinVar PMID:21057504 PMID:22499348 PMID:25326637 PMID:27233227 PMID:28492532 NCBI chr 4:119,572,669...119,626,852 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 16091
    Pathological Conditions, Signs and Symptoms 8761
      Pathologic Processes 6176
        Muscle Weakness 80
          nuclear type mitochondrial complex I deficiency 20 2
Path 2
Term Annotations click to browse term
  disease 16091
    disease of anatomical entity 15341
      cardiovascular system disease 4370
        vascular disease 3315
          artery disease 2363
            aortic disease 597
              aortic valve disease 293
                aortic valve stenosis 268
                  subvalvular aortic stenosis 213
                    hypertrophic cardiomyopathy 212
                      nuclear type mitochondrial complex I deficiency 20 2
paths to the root