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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
IEA
DNA:missense mutation:cds: MouseDO PMID:24216484 RGD:9681452 NCBI chr 1:91,928,779...92,195,702
Ensembl chr 1:91,928,779...92,195,699
JBrowse link
G Uts2 urotensin 2 ISO CTD Direct Evidence: marker/mechanism CTD PMID:16160878 NCBI chr 4:150,997,097...151,001,810
Ensembl chr 4:150,997,097...151,001,810
JBrowse link
anorexia nervosa term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Akap6 A kinase (PRKA) anchor protein 6 susceptibility ISO DNA:SNP: :rs2383378(human) RGD PMID:21079607 RGD:14349024 NCBI chr12:52,698,588...53,155,568
Ensembl chr12:52,699,383...53,155,599
JBrowse link
G Htr2a 5-hydroxytryptamine (serotonin) receptor 2A susceptibility ISO CTD Direct Evidence: marker/mechanism OMIM
CTD
NCBI chr14:74,640,874...74,706,859
Ensembl chr14:74,640,840...74,709,494
JBrowse link
G Htr4 5 hydroxytryptamine (serotonin) receptor 4 IEA MouseDO NCBI chr18:62,323,546...62,503,027
Ensembl chr18:62,324,204...62,496,577
JBrowse link
G Igfals insulin-like growth factor binding protein, acid labile subunit ISO protein:decreased expression:serum RGD PMID:11248743 RGD:12910859 NCBI chr17:24,877,844...24,882,011
Ensembl chr17:24,865,997...24,882,010
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 chr18:39,410,545...39,519,421
Ensembl chr18:39,410,545...39,519,421
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 (brain) ISO CTD Direct Evidence: marker/mechanism CTD PMID:23072421 NCBI chr 4:33,923,171...33,948,831
Ensembl chr 4:33,924,593...33,948,831
JBrowse link
G Drd1 dopamine receptor D1 ISO RGD PMID:28821448 RGD:13506951 NCBI chr13:54,051,183...54,055,658
Ensembl chr13:54,051,183...54,055,705
JBrowse link
G Drd2 dopamine receptor D2 ISO RGD PMID:28821448 RGD:13506951 NCBI chr 9:49,340,360...49,408,177
Ensembl chr 9:49,340,627...49,408,177
JBrowse link
G Drd4 dopamine receptor D4 ISO RGD PMID:28821448 RGD:13506951 NCBI chr 7:141,291,974...141,296,464
Ensembl chr 7:141,292,006...141,296,464
JBrowse link
G Mc4r melanocortin 4 receptor ISO RGD PMID:12646666 RGD:1600752 NCBI chr18:66,857,705...66,860,487
Ensembl chr18:66,857,704...66,860,506
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 chr16:18,406,882...18,426,716
Ensembl chr16:18,406,886...18,426,852
JBrowse link
G Lmna lamin A 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 chr 3:88,481,148...88,509,932
Ensembl chr 3:88,480,147...88,509,956
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, BEN and BTB (POZ) domain containing ISO ClinVar Annotator: match by term: Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination OMIM
ClinVar
PMID:24896178, PMID:25363768, PMID:25741868, PMID:28132692 NCBI chr 8:84,670,477...84,687,862
Ensembl chr 8:84,670,479...84,687,902
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13395
    disease of anatomical entity 12871
      nervous system disease 10430
        central nervous system disease 8793
          brain disease 8131
            disease of mental health 5950
              eating disorder 15
                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 + 5
                bulimia nervosa + 2
                pica disease 0
                rumination disorder 0
Path 2
Term Annotations click to browse term
  disease 13395
    disease of anatomical entity 12871
      nervous system disease 10430
        central nervous system disease 8793
          brain disease 8131
            disease of mental health 5950
              developmental disorder of mental health 3199
                specific developmental disorder 2323
                  eating disorder 15
                    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 + 5
                    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.