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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 IAGP
ISS
DNA:missense mutation:cds: MouseDO PMID:24216484 RGD:9681452 NCBI chr 2:239,048,168...239,401,649
Ensembl chr 2:239,048,168...239,401,654
JBrowse link
G UTS2 urotensin 2 EXP CTD Direct Evidence: marker/mechanism CTD PMID:16160878 NCBI chr 1:7,846,345...7,913,615
Ensembl chr 1:7,843,083...7,853,512
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 IAGP DNA:SNP: :rs2383378(human) RGD PMID:21079607 RGD:14349024 NCBI chr14:32,203,610...32,837,684
Ensembl chr14:32,329,298...32,837,684
JBrowse link
G HTR2A 5-hydroxytryptamine receptor 2A susceptibility IAGP
EXP
CTD Direct Evidence: marker/mechanism OMIM
CTD
NCBI chr13:46,831,546...46,898,082
Ensembl chr13:46,831,550...46,897,076
JBrowse link
G HTR4 5-hydroxytryptamine receptor 4 ISS MouseDO NCBI chr 5:148,451,032...148,654,527
Ensembl chr 5:148,451,032...148,677,235
JBrowse link
G IGFALS insulin like growth factor binding protein acid labile subunit IEP protein:decreased expression:serum RGD PMID:11248743 RGD:12910859 NCBI chr16:1,790,413...1,794,908
Ensembl chr16:1,790,413...1,794,971
JBrowse link
G NR3C1 nuclear receptor subfamily 3 group C member 1 IDA protein:decreased activity:blood, mononuclear leukocyte RGD PMID:10356629 RGD:7174723 NCBI chr 5:143,277,931...143,435,512
Ensembl chr 5:143,277,931...143,435,512
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 EXP CTD Direct Evidence: marker/mechanism CTD PMID:23072421 NCBI chr 6:88,139,864...88,167,349
Ensembl chr 6:88,139,864...88,166,359
JBrowse link
G DRD1 dopamine receptor D1 ISO RGD PMID:28821448 RGD:13506951 NCBI chr 5:175,440,036...175,444,182
Ensembl chr 5:175,440,036...175,444,182
JBrowse link
G DRD2 dopamine receptor D2 ISO RGD PMID:28821448 RGD:13506951 NCBI chr11:113,409,605...113,475,398
Ensembl chr11:113,409,605...113,475,691
JBrowse link
G DRD4 dopamine receptor D4 ISO RGD PMID:28821448 RGD:13506951 NCBI chr11:637,269...640,706
Ensembl chr11:637,269...640,706
JBrowse link
G MC4R melanocortin 4 receptor IAGP RGD PMID:12646666 RGD:1600752 NCBI chr18:60,371,062...60,372,775
Ensembl chr18:60,371,062...60,372,775
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 IAGP DNA:SNPs,haplotype: RGD PMID:21300128 RGD:13451125 NCBI chr22:19,941,772...19,969,975
Ensembl chr22:19,941,733...19,969,975
Ensembl chr22:19,941,733...19,969,975
JBrowse link
G LMNA lamin A/C IAGP 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 1:156,082,573...156,140,081
Ensembl chr 1:156,082,573...156,140,089
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 IAGP 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 chr19:13,116,848...13,141,147
Ensembl chr19:13,116,862...13,141,147
JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18836
    disease of anatomical entity 17322
      nervous system disease 13416
        central nervous system disease 11456
          brain disease 10641
            disease of mental health 8151
              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 18836
    disease of anatomical entity 17322
      nervous system disease 13416
        central nervous system disease 11456
          brain disease 10641
            disease of mental health 8151
              developmental disorder of mental health 4718
                specific developmental disorder 2763
                  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.