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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:eating disorder
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Accession:DOID:8670 term browser browse the term
Definition:A group of disorders characterized by physiological and psychological disturbances in appetite or food intake.
Synonyms:exact_synonym: Appetite Disorder;   Appetite Disorders;   Eating Disorders;   Feeding Disorder;   Feeding Disorders;   Feeding and Eating Disorders
 primary_id: MESH:D001068
 alt_id: RDO:0001861
 xref: ICD10CM:F50;   ICD9CM:307.50;   NCI:C89332
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
eating disorder term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Hdac4 histone deacetylase 4 ISO DNA:missense mutation:cds: RGD PMID:24216484 RGD:9681452 NCBI chrNW_004936745:1,730,743...1,942,071 JBrowse link
G Uts2 urotensin 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:16160878 NCBI chrNW_004936623:2,339,259...2,345,717 JBrowse link
anorexia nervosa term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Akap6 A-kinase anchoring protein 6 susceptibility ISO DNA:SNP: :rs2383378(human) RGD PMID:21079607 RGD:14349024 NCBI chrNW_004936494:6,744,923...7,228,670 JBrowse link
G Htr2a 5-hydroxytryptamine receptor 2A susceptibility ISO CTD Direct Evidence: marker/mechanism OMIM
CTD
NCBI chrNW_004936565:335,238...394,683 JBrowse link
G Igfals insulin like growth factor binding protein acid labile subunit ISO protein:decreased expression:serum RGD PMID:11248743 RGD:12910859 NCBI chrNW_004936694:2,205,294...2,207,343 JBrowse link
G Nr3c1 nuclear receptor subfamily 3 group C member 1 ISO protein:decreased activity:blood, mononuclear leukocyte RGD PMID:10356629 RGD:7174723 NCBI chrNW_004936504:10,960,069...11,056,834 JBrowse link
Binge-Eating Disorder term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cnr1 cannabinoid receptor 1 ISO CTD Direct Evidence: marker/mechanism CTD PMID:23072421 NCBI chrNW_004936510:3,779,930...3,806,615 JBrowse link
G Drd1 dopamine receptor D1 ISO RGD PMID:28821448 RGD:13506951 NCBI chrNW_004936609:790,647...795,187 JBrowse link
G Drd2 dopamine receptor D2 ISO RGD PMID:28821448 RGD:13506951 NCBI chrNW_004936612:1,094,686...1,154,149 JBrowse link
G Drd4 dopamine receptor D4 ISO RGD PMID:28821448 RGD:13506951 NCBI chrNW_004936888:468,334...471,254 JBrowse link
G Mc4r melanocortin 4 receptor ISO RGD PMID:12646666 RGD:1600752 NCBI chrNW_004936497:4,636,370...4,638,205 JBrowse link
bulimia nervosa term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Comt catechol-O-methyltransferase susceptibility ISO DNA:SNPs,haplotype: RGD PMID:21300128 RGD:13451125 NCBI chrNW_004936619:3,847,059...3,883,866 JBrowse link
G Lmna lamin A/C ISO ClinVar Annotator: match by term: Bulimia nervosa, age of onset of weight loss in ClinVar PMID:2526018, PMID:10739751, PMID:11102973, PMID:11180602, PMID:15060110, PMID:15770669, PMID:16585054, PMID:18478590, PMID:18795223, PMID:18926329, PMID:19875404, PMID:20497714, PMID:20848652, PMID:21831885, PMID:21980471, PMID:22177269, PMID:22199124, PMID:22276265, PMID:22355414, PMID:22526018, PMID:22570643, PMID:23349452, PMID:23861362, PMID:24033266, PMID:24503780, PMID:24623722, PMID:25025039, PMID:25448463, PMID:25637381, PMID:25741868, PMID:25873806, PMID:26467025, PMID:26498160, PMID:27000522, PMID:27153395, PMID:27447704, PMID:27896284, PMID:28087566, PMID:28492532, PMID:28663758, PMID:28701371, PMID:28807990, PMID:30311386 NCBI chrNW_004936580:5,374,208...5,395,442 JBrowse link
Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Nacc1 nucleus accumbens associated 1 ISO OMIM NCBI chrNW_004936659:2,164,147...2,169,879 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11943
    disease of anatomical entity 11504
      nervous system disease 9435
        central nervous system disease 7979
          brain disease 7385
            disease of mental health 5363
              eating disorder 14
                Binge-Eating Disorder 5
                Female Athlete Triad Syndrome 0
                Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination 1
                Pointer Syndrome 0
                anorexia nervosa + 4
                bulimia nervosa + 2
                pica disease 0
                rumination disorder 0
Path 2
Term Annotations click to browse term
  disease 11943
    disease of anatomical entity 11504
      nervous system disease 9435
        central nervous system disease 7979
          brain disease 7385
            disease of mental health 5363
              developmental disorder of mental health 2907
                specific developmental disorder 2181
                  eating disorder 14
                    Binge-Eating Disorder 5
                    Female Athlete Triad Syndrome 0
                    Neurodevelopmental Disorder with Epilepsy, Cataracts, Feeding Difficulties, and Delayed Brain Myelination 1
                    Pointer Syndrome 0
                    anorexia nervosa + 4
                    bulimia nervosa + 2
                    pica disease 0
                    rumination disorder 0
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.