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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 56,923,115 56,978,067 RGD:9068941
G CALHM5 calcium homeostasis modulator family member 5 JBrowse link 1 56,928,836 56,934,196 RGD:9068941
G CALHM6 calcium homeostasis modulator family member 6 JBrowse link 1 56,894,565 56,896,665 RGD:9068941
G COL10A1 collagen type X alpha 1 chain JBrowse link 12 71,803,372 71,810,049 RGD:9068941
G DCBLD1 discoidin, CUB and LCCL domain containing 1 JBrowse link 1 57,733,681 57,809,624 RGD:9068941
G DSE dermatan sulfate epimerase JBrowse link 1 56,787,809 56,868,037 RGD:9068941
G FAM162B family with sequence similarity 162 member B JBrowse link 1 57,159,367 57,169,533 RGD:9068941
G FRK fyn related Src family tyrosine kinase JBrowse link 12 71,659,397 71,756,213 RGD:9068941
G GOPC golgi associated PDZ and coiled-coil motif containing JBrowse link 1 57,790,118 57,829,022 RGD:9068941
G GPRC6A G protein-coupled receptor class C group 6 member A JBrowse link 1 57,191,210 57,212,008 RGD:9068941
G HDAC2 histone deacetylase 2 JBrowse link 12 70,053,822 70,083,491 RGD:9068941
G HS3ST5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link 12 70,137,232 70,387,797 RGD:9068941
G KPNA5 karyopherin subunit alpha 5 JBrowse link 1 57,112,204 57,154,865 RGD:9068941
G LAMA4 laminin subunit alpha 4 JBrowse link 12 68,535,614 68,639,115 RGD:9068941
G MARCKS myristoylated alanine rich protein kinase C substrate JBrowse link 12 69,980,003 69,987,150 RGD:9068941
G NT5DC1 5'-nucleotidase domain containing 1 JBrowse link 12 71,790,973 71,909,109 RGD:9068941
G NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link 1 57,866,760 57,895,505 RGD:9068941
G RFPL4B ret finger protein like 4B JBrowse link 12 68,753,605 68,757,164 RGD:9068941
G RFX6 regulatory factor X6 JBrowse link 1 57,242,563 57,297,300 RGD:9068941
G ROS1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link 1 57,555,278 57,677,541 RGD:9068941
G RSPH4A radial spoke head component 4A JBrowse link 1 57,063,752 57,079,289 RGD:9068941
G RWDD1 RWD domain containing 1 JBrowse link 1 56,986,809 57,008,720 RGD:9068941
G TRAPPC3L trafficking protein particle complex 3 like JBrowse link 1 56,922,018 56,986,818 RGD:9068941
G TSPYL1 TSPY like 1 JBrowse link 12 71,933,904 71,937,508 RGD:9068941
G TSPYL4 TSPY like 4 JBrowse link 12 71,916,682 71,918,481 RGD:9068941
G USP9X ubiquitin specific peptidase 9 X-linked JBrowse link X 35,522,873 35,676,086 RGD:9068941
G VGLL2 vestigial like family member 2 JBrowse link 1 57,529,901 57,537,893 RGD:9068941
G ZUP1 zinc finger containing ubiquitin peptidase 1 JBrowse link 1 57,076,730 57,108,527 RGD:9068941
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DBH dopamine beta-hydroxylase JBrowse link 9 50,004,806 50,024,130 RGD:7240710
G HSPA5 heat shock protein family A (Hsp70) member 5 JBrowse link 9 57,850,870 57,855,607 RGD:9068941
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 2 60,319,304 60,362,532 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 14 13,644,891 13,852,829 RGD:9068941
G GNAS GNAS complex locus JBrowse link 24 43,643,409 43,658,641 RGD:9068941
G GNB3 G protein subunit beta 3 JBrowse link 27 38,175,928 38,182,473 RGD:9068941
G MT-ND2 mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 JBrowse link MT 3,914 4,955 RGD:9068941
G OPRD1 opioid receptor delta 1 JBrowse link 2 71,685,129 71,721,692 RGD:9068941
G OPRM1 opioid receptor mu 1 JBrowse link 1 43,972,915 44,037,477 RGD:9068941
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CYB561 cytochrome b561 JBrowse link 9 11,461,738 11,474,413 RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 2 60,319,304 60,362,532 RGD:7240710
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NPPB natriuretic peptide B JBrowse link 2 84,395,844 84,397,473 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12605
    disease of anatomical entity 12148
      nervous system disease 9872
        Neurologic Manifestations 3720
          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 12605
    disease of anatomical entity 12148
      nervous system disease 9872
        central nervous system disease 8268
          brain disease 7606
            disease of mental health 5478
              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.