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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_004936824 1,098,792 1,103,607 RGD:9068941
G Calhm5 calcium homeostasis modulator family member 5 JBrowse link NW_004936824 1,056,082 1,061,368 RGD:9068941
G Calhm6 calcium homeostasis modulator family member 6 JBrowse link NW_004936824 1,019,124 1,020,871 RGD:9068941
G Col10a1 collagen type X alpha 1 chain JBrowse link NW_004936824 734,499 741,674 RGD:9068941
G Dcbld1 discoidin, CUB and LCCL domain containing 1 JBrowse link NW_004936658 547,245 606,540 RGD:9068941
G Dse dermatan sulfate epimerase JBrowse link NW_004936824 957,783 995,465 RGD:9068941
G Fam162b family with sequence similarity 162 member B JBrowse link NW_004936658 7,938 13,751 RGD:9068941
G Frk fyn related Src family tyrosine kinase JBrowse link NW_004936824 575,618 677,775 RGD:9068941
G Gopc golgi associated PDZ and coiled-coil motif containing JBrowse link NW_004936658 614,711 655,874 RGD:9068941
G Gprc6a G protein-coupled receptor class C group 6 member A JBrowse link NW_004936658 38,931 58,534 RGD:9068941
G Hdac2 histone deacetylase 2 JBrowse link NW_004936679 2,448,676 2,474,641 RGD:9068941
G Hs3st5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link NW_004936679 2,540,894 2,737,462 RGD:9068941
G Lama4 laminin subunit alpha 4 JBrowse link NW_004936679 803,131 938,022 RGD:9068941
G Marcks myristoylated alanine rich protein kinase C substrate JBrowse link NW_004936679 2,373,104 2,379,230 RGD:9068941
G Nt5dc1 5'-nucleotidase domain containing 1 JBrowse link NW_004936824 805,647 841,113 RGD:9068941
G Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link NW_004936658 695,431 718,891 RGD:9068941
G Rfpl4b ret finger protein like 4B JBrowse link NW_004936679 1,057,682 1,058,497 RGD:9068941
G Rfx6 regulatory factor X6 JBrowse link NW_004936658 94,589 145,135 RGD:9068941
G Ros1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link NW_004936658 382,025 506,818 RGD:9068941
G Rsph4a radial spoke head component 4A JBrowse link NW_004937068 45,105 59,540 RGD:9068941
G Rwdd1 RWD domain containing 1 JBrowse link NW_004936824 1,117,865 1,136,974 RGD:9068941
G Trappc3l trafficking protein particle complex 3 like JBrowse link NW_004936824 1,048,636 1,090,900 RGD:9068941
G Tspyl1 TSPY like 1 JBrowse link NW_004936824 857,696 860,604 RGD:9068941
G Tspyl4 TSPY like 4 JBrowse link NW_004936824 842,698 846,653 RGD:9068941
G Usp9x ubiquitin specific peptidase 9 X-linked JBrowse link NW_004936502 7,649,808 7,732,731 RGD:9068941
G Vgll2 vestigial like family member 2 JBrowse link NW_004936658 362,377 370,298 RGD:9068941
G Zup1 zinc finger containing ubiquitin peptidase 1 JBrowse link NW_004937068 21,312 42,266 RGD:9068941
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dbh dopamine beta-hydroxylase JBrowse link NW_004936669 3,302,014 3,326,233 RGD:7240710
G Hspa5 heat shock protein family A (Hsp70) member 5 JBrowse link NW_004936487 13,348,465 13,352,717 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_004936475 7,937,920 7,973,563 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_004936763 1,225,355 1,308,257 RGD:9068941
G Gnas GNAS complex locus JBrowse link NW_004936530 1,353,432 1,407,437 RGD:9068941
G Gnb3 G protein subunit beta 3 JBrowse link NW_004936709 970,169 977,059 RGD:9068941
G Oprd1 opioid receptor delta 1 JBrowse link NW_004936474 12,860,293 12,902,389 RGD:9068941
G Oprm1 opioid receptor mu 1 JBrowse link NW_004936489 6,506,207 6,567,136 RGD:9068941
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LOC101968635 cytochrome b561 JBrowse link NW_004936541 4,123,187 4,130,819 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_004936475 7,937,920 7,973,563 RGD:7240710
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nppb natriuretic peptide B JBrowse link NW_004936474 683,325 684,662 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11879
    disease of anatomical entity 11444
      nervous system disease 9331
        Neurologic Manifestations 3555
          somatoform disorder 37
            Neurasthenia 0
            body dysmorphic disorder 27
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 10
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 11879
    disease of anatomical entity 11444
      nervous system disease 9331
        central nervous system disease 7822
          brain disease 7189
            disease of mental health 5126
              somatoform disorder 37
                Neurasthenia 0
                body dysmorphic disorder 27
                conversion disorder 0
                hypochondriasis 0
                neurocirculatory asthenia + 10
                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.