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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:anorexia nervosa
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Accession:DOID:8689 term browser browse the term
Definition:An eating disorder that is characterized by the lack or loss of APPETITE, known as ANOREXIA. Other features include excess fear of becoming OVERWEIGHT; BODY IMAGE disturbance; significant WEIGHT LOSS; refusal to maintain minimal normal weight; and AMENORRHEA. This disorder occurs most frequently in adolescent females. (APA, Thesaurus of Psychological Index Terms, 1994)
Synonyms:exact_synonym: AN;   ANON;   ANON1;   ANOREXIA NERVOSA, SUSCEPTIBILITY TO;   ANOREXIA NERVOSA, SUSCEPTIBILITY TO, 1;   Anorexia Nervosas
 primary_id: MESH:D000856
 alt_id: OMIM:606788;   RDO:0004857
 xref: ICD10CM:F50.0;   ICD9CM:307.1;   NCI:C34387
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
 
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

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11962
    disease of anatomical entity 11526
      nervous system disease 9457
        central nervous system disease 8005
          brain disease 7410
            disease of mental health 5397
              eating disorder 13
                anorexia nervosa 4
                  ANOREXIA NERVOSA 2 0
Path 2
Term Annotations click to browse term
  disease 11962
    disease of anatomical entity 11526
      nervous system disease 9457
        central nervous system disease 8005
          brain disease 7410
            disease of mental health 5397
              developmental disorder of mental health 2936
                specific developmental disorder 2214
                  eating disorder 13
                    anorexia nervosa 4
                      ANOREXIA NERVOSA 2 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.