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ONTOLOGY REPORT - ANNOTATIONS


Term:somatoform disorder
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Accession:DOID:4737 term browser browse the term
Definition:Disorders having the presence of physical symptoms that suggest a general medical condition but that are not fully explained by another medical condition, by the direct effects of a substance, or by another mental disorder. The MEDICALLY UNEXPLAINED SYMPTOMS must cause clinically significant distress or impairment in social, occupational, or other areas of functioning. In contrast to FACTITIOUS DISORDERS and MALINGERING, the physical symptoms are not under voluntary control. (APA, DSM-V)
Synonyms:exact_synonym: Briquet syndrome;   Pain Disorder;   Psychophysiological Disorder;   Psychophysiological Disorders;   medically unexplained syndrome;   medically unexplained syndromes;   physiological malfunction arising from mental factor;   psychophysiologic disorder;   psychophysiologic disorders;   psychosomatic disorder;   psychosomatic disorders;   somatoform disorders
 primary_id: MESH:D011602;   MESH:D013001
 xref: ICD10CM:F45;   ICD10CM:F45.9;   ICD9CM:300.8;   NCI:C34956
For additional species annotation, visit the Alliance of Genome Resources.


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body dysmorphic disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Calhm4 calcium homeostasis modulator family member 4 JBrowse link NW_004955526 126,100 137,551 RGD:9068941
G Calhm5 calcium homeostasis modulator family member 5 JBrowse link NW_004955526 203,971 213,328 RGD:9068941
G Calhm6 calcium homeostasis modulator family member 6 JBrowse link NW_004955526 319,920 321,985 RGD:9068941
G Col10a1 collagen type X alpha 1 chain JBrowse link NW_004955526 641,577 679,295 RGD:9068941
G Dcbld1 discoidin, CUB and LCCL domain containing 1 JBrowse link NW_004955436 688,546 726,952 RGD:9068941
G Dse dermatan sulfate epimerase JBrowse link NW_004955526 348,673 393,328 RGD:9068941
G Fam162b family with sequence similarity 162 member B JBrowse link NW_004955436 106,648 110,279 RGD:9068941
G Frk fyn related Src family tyrosine kinase JBrowse link NW_004955526 736,446 892,331 RGD:9068941
G Gopc golgi associated PDZ and coiled-coil motif containing JBrowse link NW_004955436 743,616 777,878 RGD:9068941
G Gprc6a G protein-coupled receptor class C group 6 member A JBrowse link NW_004955436 137,809 159,481 RGD:9068941
G Hdac2 histone deacetylase 2 JBrowse link NW_004955526 2,739,099 2,759,640 RGD:9068941
G Hs3st5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link NW_004955526 2,418,217 2,652,025 RGD:9068941
G Kpna5 karyopherin subunit alpha 5 JBrowse link NW_004955436 48,880 102,447 RGD:9068941
G Lama4 laminin subunit alpha 4 JBrowse link NW_004955526 4,330,388 4,465,810 RGD:9068941
G Nt5dc1 5'-nucleotidase domain containing 1 JBrowse link NW_004955526 568,307 604,941 RGD:9068941
G Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link NW_004955436 825,387 850,558 RGD:9068941
G Rfpl4b ret finger protein like 4B JBrowse link NW_004955526 4,242,108 4,253,095 RGD:9068941
G Rfx6 regulatory factor X6 JBrowse link NW_004955436 213,810 278,699 RGD:9068941
G Ros1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link NW_004955436 528,038 636,194 RGD:9068941
G Rsph4a radial spoke head component 4A JBrowse link NW_004955436 30,638 43,581 RGD:9068941
G Rwdd1 RWD domain containing 1 JBrowse link NW_004955526 94,518 120,421 RGD:9068941
G Trappc3l trafficking protein particle complex 3 like JBrowse link NW_004955526 120,620 217,855 RGD:9068941
G Tspyl1 TSPY like 1 JBrowse link NW_004955526 539,178 552,120 RGD:9068941
G Tspyl4 TSPY like 4 JBrowse link NW_004955526 562,891 567,892 RGD:9068941
G Usp9x ubiquitin specific peptidase 9 X-linked JBrowse link NW_004955565 1,479,040 1,602,070 RGD:9068941
G Vgll2 vestigial like family member 2 JBrowse link NW_004955436 510,478 514,511 RGD:9068941
G Zup1 zinc finger containing ubiquitin peptidase 1 JBrowse link NW_004955436 1,001 28,469 RGD:9068941
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dbh dopamine beta-hydroxylase JBrowse link NW_004955513 2,918,085 2,932,481 RGD:7240710
G Hspa5 heat shock protein family A (Hsp70) member 5 JBrowse link NW_004955419 3,055,420 3,060,208 RGD:9068941
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc6a2 solute carrier family 6 member 2 JBrowse link NW_004955433 13,170,986 13,216,270 RGD:9068941
Orthostatic Hypotension term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcb1 ATP binding cassette subfamily B member 1 JBrowse link NW_004955432 4,911,774 5,085,349 RGD:9068941
G Gnb3 G protein subunit beta 3 JBrowse link NW_004955413 4,440,693 4,447,419 RGD:9068941
G Oprd1 opioid receptor delta 1 JBrowse link NW_004955452 7,866,790 7,913,399 RGD:9068941
G Oprm1 opioid receptor mu 1 JBrowse link NW_004955439 7,870,563 7,923,817 RGD:9068941
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC102028532 cytochrome b561 JBrowse link NW_004955478 8,362,190 8,366,947 RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc6a2 solute carrier family 6 member 2 JBrowse link NW_004955433 13,170,986 13,216,270 RGD:7240710
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nppb natriuretic peptide B JBrowse link NW_004955486 2,054,775 2,056,130 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11744
    disease of anatomical entity 11304
      nervous system disease 9202
        Neurologic Manifestations 3500
          somatoform disorder 36
            Neurasthenia 0
            body dysmorphic disorder 27
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 9
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 11744
    disease of anatomical entity 11304
      nervous system disease 9202
        central nervous system disease 7728
          brain disease 7097
            disease of mental health 5065
              somatoform disorder 36
                Neurasthenia 0
                body dysmorphic disorder 27
                conversion disorder 0
                hypochondriasis 0
                neurocirculatory asthenia + 9
                pain disorder 0
                somatization 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.