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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 1 82,109,535 82,154,349 RGD:9068941
G CALHM5 calcium homeostasis modulator family member 5 JBrowse link 1 82,109,042 82,119,480 RGD:9068941
G CALHM6 calcium homeostasis modulator family member 6 JBrowse link 1 82,085,781 82,087,897 RGD:9068941
G COL10A1 collagen type X alpha 1 chain JBrowse link 1 81,766,829 81,773,818 RGD:9068941
G DCBLD1 discoidin, CUB and LCCL domain containing 1 JBrowse link 1 44,301,108 44,373,712 RGD:9068941
G DSE dermatan sulfate epimerase JBrowse link 1 81,996,894 82,063,847 RGD:9068941
G FAM162B family with sequence similarity 162 member B JBrowse link 1 44,889,582 44,897,184 RGD:9068941
G FRK fyn related Src family tyrosine kinase JBrowse link 1 81,606,599 81,714,543 RGD:9068941
G GOPC golgi associated PDZ and coiled-coil motif containing JBrowse link 1 44,239,364 44,285,886 RGD:9068941
G GPRC6A G protein-coupled receptor class C group 6 member A JBrowse link 1 44,852,731 44,875,518 RGD:9068941
G HDAC2 histone deacetylase 2 JBrowse link 1 79,867,713 79,901,597 RGD:9068941
G HS3ST5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link 1 79,956,485 80,140,140 RGD:9068941
G KPNA5 karyopherin subunit alpha 5 JBrowse link 1 44,900,495 44,941,219 RGD:9068941
G LAMA4 laminin subunit alpha 4 JBrowse link 1 78,071,990 78,224,564 RGD:9068941
G MARCKS myristoylated alanine rich protein kinase C substrate JBrowse link 1 79,789,796 79,795,895 RGD:9068941
G NT5DC1 5'-nucleotidase domain containing 1 JBrowse link 1 81,745,918 81,880,691 RGD:9068941
G NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link 1 44,156,771 44,186,224 RGD:9068941
G RFPL4B ret finger protein like 4B JBrowse link 1 78,312,248 78,313,153 RGD:9068941
G RFX6 regulatory factor X6 JBrowse link 1 44,765,451 44,826,884 RGD:9068941
G ROS1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link 1 44,409,877 44,535,784 RGD:9068941
G RSPH4A radial spoke head component 4A JBrowse link 1 44,964,433 45,004,925 RGD:9068941
G RWDD1 RWD domain containing 1 JBrowse link 1 82,161,371 82,180,325 RGD:9068941
G TRAPPC3L trafficking protein particle complex 3 like JBrowse link 1 82,100,970 82,145,418 RGD:9068941
G TSPYL1 TSPY like 1 JBrowse link 1 81,906,168 81,909,461 RGD:9068941
G TSPYL4 TSPY like 4 JBrowse link 1 81,888,946 81,893,643 RGD:9068941
G USP9X ubiquitin specific peptidase 9 X-linked JBrowse link X 36,736,049 36,888,702 RGD:9068941
G VGLL2 vestigial like family member 2 JBrowse link 1 44,549,407 44,557,793 RGD:9068941
G ZUP1 zinc finger containing ubiquitin peptidase 1 JBrowse link 1 44,939,914 45,013,764 RGD:9068941
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DBH dopamine beta-hydroxylase JBrowse link 1 273,204,407 273,225,562 RGD:7240710
G HSPA5 heat shock protein family A (Hsp70) member 5 JBrowse link 1 265,930,044 265,934,959 RGD:9068941
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 6 29,931,650 29,981,636 RGD:9068941
Orthostatic Hypotension term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 JBrowse link 9 93,049,955 93,146,469 RGD:9068941
G GNAS GNAS complex locus JBrowse link 17 58,985,580 59,053,022 RGD:9068941
G GNB3 G protein subunit beta 3 JBrowse link 5 63,863,656 63,871,352 RGD:9068941
G ND2 NADH dehydrogenase subunit 2 JBrowse link MT 5,087 6,128 RGD:9068941
G OPRD1 opioid receptor delta 1 JBrowse link 6 85,775,576 85,827,170 RGD:9068941
G OPRM1 opioid receptor mu 1 JBrowse link 1 12,634,125 12,702,295 RGD:9068941
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CYB561 cytochrome b561 JBrowse link 12 15,435,973 15,447,104 RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 6 29,931,650 29,981,636 RGD:7240710
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NPPB natriuretic peptide B JBrowse link 6 71,930,374 71,931,843 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12552
    disease of anatomical entity 12088
      nervous system disease 9812
        Neurologic Manifestations 3699
          somatoform disorder 39
            Neurasthenia 0
            body dysmorphic disorder 28
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 11
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 12552
    disease of anatomical entity 12088
      nervous system disease 9812
        central nervous system disease 8232
          brain disease 7566
            disease of mental health 5440
              somatoform disorder 39
                Neurasthenia 0
                body dysmorphic disorder 28
                conversion disorder 0
                hypochondriasis 0
                neurocirculatory asthenia + 11
                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.