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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:Hypoinsulinemia
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Accession:DOID:9002188 term browser browse the term
Definition:A decreased concentration of insulin in the blood.
Synonyms:primary_id: RDO:9000335



show annotations for term's descendants           Sort by:
Hypoinsulinemia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ins1 insulin 1 ISO ClinVar Annotator: match by term: Hypoinsulinemia ClinVar PMID:12610512 PMID:25741868 PMID:26467025 PMID:33206859 NCBI chr 1:251,244,973...251,245,540
Ensembl chr 1:251,244,973...251,245,536
JBrowse link
G Ins2 insulin 2 ISO ClinVar Annotator: match by term: Hypoinsulinemia ClinVar PMID:12610512 PMID:25741868 PMID:26467025 PMID:33206859 NCBI chr 1:197,843,277...197,992,522
Ensembl chr 1:197,843,281...197,864,775
JBrowse link
G Neurod1 neuronal differentiation 1 ISO ClinVar Annotator: match by term: Hypoinsulinemia ClinVar PMID:12639765 PMID:18414213 PMID:25741868 PMID:27420379 PMID:28492532 NCBI chr 3:64,359,554...64,363,526
Ensembl chr 3:64,359,395...64,363,649
JBrowse link
G Th tyrosine hydroxylase ISO ClinVar Annotator: match by term: Hypoinsulinemia ClinVar PMID:12610512 PMID:25741868 PMID:26467025 PMID:33206859 NCBI chr 1:198,071,500...198,078,832
Ensembl chr 1:198,071,503...198,109,767
JBrowse link
G Ucp3 uncoupling protein 3 ISO RGD PMID:10935638 RGD:737762 NCBI chr 1:154,815,777...154,828,764
Ensembl chr 1:154,815,777...154,828,762
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 21128
    Nutritional and Metabolic Diseases 8237
      disease of metabolism 8237
        inherited metabolic disorder 6214
          carbohydrate metabolic disorder 3267
            glucose metabolism disease 2071
              Hypoinsulinemia 6
Path 2
Term Annotations click to browse term
  disease 21128
    Developmental Disease 18449
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 18309
        genetic disease 18253
          inherited metabolic disorder 6214
            carbohydrate metabolic disorder 3267
              glucose metabolism disease 2071
                Hypoinsulinemia 6
paths to the root