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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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somatoform disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G IFNA2 interferon alpha 2 JBrowse link 9 21,384,255 21,385,398 RGD:11554173
body dysmorphic disorder term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CALHM4 calcium homeostasis modulator family member 4 JBrowse link 6 116,529,021 116,561,127 RGD:8554872
G CALHM5 calcium homeostasis modulator family member 5 JBrowse link 6 116,511,639 116,524,788 RGD:8554872
G CALHM6 calcium homeostasis modulator family member 6 JBrowse link 6 116,461,375 116,463,782 RGD:8554872
G COL10A1 collagen type X alpha 1 chain JBrowse link 6 116,118,909 116,219,937 RGD:8554872
G DCBLD1 discoidin, CUB and LCCL domain containing 1 JBrowse link 6 117,480,351 117,569,858 RGD:8554872
G DSE dermatan sulfate epimerase JBrowse link 6 116,254,171 116,444,861 RGD:8554872
G FAM162B family with sequence similarity 162 member B JBrowse link 6 116,752,197 116,765,719 RGD:8554872
G FRK fyn related Src family tyrosine kinase JBrowse link 6 115,931,149 116,100,739 RGD:8554872
G GOPC golgi associated PDZ and coiled-coil motif containing JBrowse link 6 117,560,269 117,602,520 RGD:8554872
G GPRC6A G protein-coupled receptor class C group 6 member A JBrowse link 6 116,788,512 116,831,128 RGD:8554872
G HDAC2 histone deacetylase 2 JBrowse link 6 113,933,028 113,971,148 RGD:8554872
G HS3ST5 heparan sulfate-glucosamine 3-sulfotransferase 5 JBrowse link 6 114,055,586 114,342,395 RGD:8554872
G KPNA5 karyopherin subunit alpha 5 JBrowse link 6 116,677,643 116,741,867 RGD:8554872
G LAMA4 laminin subunit alpha 4 JBrowse link 6 112,107,931 112,254,722 RGD:8554872
G MARCKS myristoylated alanine rich protein kinase C substrate JBrowse link 6 113,857,345 113,863,475 RGD:8554872
G NT5DC1 5'-nucleotidase domain containing 1 JBrowse link 6 116,100,833 116,249,497 RGD:8554872
G NUS1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link 6 117,675,469 117,710,727 RGD:8554872
G RFPL4B ret finger protein like 4B JBrowse link 6 112,347,330 112,351,294 RGD:8554872
G RFX6 regulatory factor X6 JBrowse link 6 116,877,218 116,932,163 RGD:8554872
G ROS1 ROS proto-oncogene 1, receptor tyrosine kinase JBrowse link 6 117,287,353 117,426,065 RGD:8554872
G RSPH4A radial spoke head component 4A JBrowse link 6 116,598,184 116,633,051 RGD:8554872
G RWDD1 RWD domain containing 1 JBrowse link 6 116,571,504 116,597,675 RGD:8554872
G TRAPPC3L trafficking protein particle complex 3 like JBrowse link 6 116,494,989 116,545,684 RGD:8554872
G TSPYL1 TSPY like 1 JBrowse link 6 116,274,858 116,279,930 RGD:8554872
G TSPYL4 TSPY like 4 JBrowse link 6 116,249,964 116,254,075 RGD:8554872
G USP9X ubiquitin specific peptidase 9 X-linked JBrowse link X 41,085,420 41,236,579 RGD:8554872
G VGLL2 vestigial like family member 2 JBrowse link 6 117,265,558 117,273,565 RGD:8554872
G ZUP1 zinc finger containing ubiquitin peptidase 1 JBrowse link 6 116,635,618 116,668,810 RGD:8554872
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DBH dopamine beta-hydroxylase JBrowse link 9 133,636,363 133,659,329 RGD:8554872
RGD:7240710
G DBH-AS1 DBH antisense RNA 1 JBrowse link 9 133,654,587 133,657,408 RGD:8554872
G HSPA5 heat shock protein family A (Hsp70) member 5 JBrowse link 9 125,234,853 125,241,343 RGD:5685690
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 16 55,655,928 55,706,192 RGD:1624278
Orthostatic Hypotension term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ABCB1 ATP binding cassette subfamily B member 1 JBrowse link 7 87,503,017 87,713,323 RGD:11554173
G GNAS GNAS complex locus JBrowse link 20 58,839,681 58,911,196 RGD:1580406
G GNB3 G protein subunit beta 3 JBrowse link 12 6,840,922 6,847,393 RGD:1580406
G MT-ND2 mitochondrially encoded NADH:ubiquinone oxidoreductase core subunit 2 JBrowse link MT 4,470 5,511 RGD:1581056
G OPRD1 opioid receptor delta 1 JBrowse link 1 28,812,170 28,871,267 RGD:11554173
G OPRM1 opioid receptor mu 1 JBrowse link 6 154,010,496 154,246,867 RGD:11554173
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G CYB561 cytochrome b561 JBrowse link 17 63,432,304 63,446,306 RGD:8554872
RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 16 55,655,928 55,706,192 RGD:8554872
RGD:11554173
RGD:7240710
postural orthostatic tachycardia syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G SLC6A2 solute carrier family 6 member 2 JBrowse link 16 55,655,928 55,706,192 RGD:13592920
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NPPB natriuretic peptide B JBrowse link 1 11,857,464 11,858,945 RGD:7247623

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 17649
    disease of anatomical entity 16248
      nervous system disease 12510
        Neurologic Manifestations 4324
          somatoform disorder 41
            Neurasthenia 0
            body dysmorphic disorder 28
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 12
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 17649
    disease of anatomical entity 16248
      nervous system disease 12510
        central nervous system disease 10591
          brain disease 9780
            disease of mental health 7316
              somatoform disorder 41
                Neurasthenia 0
                body dysmorphic disorder 28
                conversion disorder 0
                hypochondriasis 0
                neurocirculatory asthenia + 12
                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.