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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 10 34,038,784 34,044,313 RGD:8554872
G Calhm5 calcium homeostasis modulator family member 5 JBrowse link 10 34,091,352 34,096,519 RGD:8554872
G Calhm6 calcium homeostasis modulator family member 6 JBrowse link 10 34,126,067 34,127,972 RGD:8554872
G Col10a1 collagen, type X, alpha 1 JBrowse link 10 34,389,981 34,397,085 RGD:8554872
G Dcbld1 discoidin, CUB and LCCL domain containing 1 JBrowse link 10 52,233,578 52,321,378 RGD:8554872
G Dse dermatan sulfate epimerase JBrowse link 10 34,151,389 34,208,282 RGD:8554872
G Fam162b family with sequence similarity 162, member B JBrowse link 10 51,585,414 51,590,592 RGD:8554872
G Frk fyn-related kinase JBrowse link 10 34,483,400 34,611,232 RGD:8554872
G Gopc golgi associated PDZ and coiled-coil motif containing JBrowse link 10 52,337,024 52,382,124 RGD:8554872
G Gprc6a G protein-coupled receptor, family C, group 6, member A JBrowse link 10 51,614,823 51,631,458 RGD:8554872
G Hdac2 histone deacetylase 2 JBrowse link 10 36,974,297 37,001,889 RGD:8554872
G Hs3st5 heparan sulfate (glucosamine) 3-O-sulfotransferase 5 JBrowse link 10 36,506,590 36,834,397 RGD:8554872
G Lama4 laminin, alpha 4 JBrowse link 10 38,965,515 39,110,188 RGD:8554872
G Marcks myristoylated alanine rich protein kinase C substrate JBrowse link 10 37,133,243 37,138,926 RGD:8554872
G Nt5dc1 5'-nucleotidase domain containing 1 JBrowse link 10 34,303,609 34,418,589 RGD:8554872
G Nus1 NUS1 dehydrodolichyl diphosphate synthase subunit JBrowse link 10 52,417,547 52,440,192 RGD:8554872
G Rfpl4b ret finger protein-like 4B JBrowse link 10 38,820,541 38,821,779 RGD:8554872
G Rfx6 regulatory factor X, 6 JBrowse link 10 51,677,760 51,730,429 RGD:8554872
G Ros1 Ros1 proto-oncogene JBrowse link 10 52,044,863 52,195,398 RGD:8554872
G Rsph4a radial spoke head 4 homolog A (Chlamydomonas) JBrowse link 10 33,905,111 33,916,021 RGD:8554872
G Rwdd1 RWD domain containing 1 JBrowse link 10 33,996,555 34,019,616 RGD:8554872
G Trappc3l trafficking protein particle complex 3 like JBrowse link 10 34,037,597 34,109,815 RGD:8554872
G Tspyl1 testis-specific protein, Y-encoded-like 1 JBrowse link 10 34,282,190 34,284,885 RGD:8554872
G Tspyl4 TSPY-like 4 JBrowse link 10 34,297,421 34,301,320 RGD:8554872
G Usp9x ubiquitin specific peptidase 9, X chromosome JBrowse link X 13,070,982 13,173,328 RGD:8554872
G Vgll2 vestigial like family member 2 JBrowse link 10 52,022,502 52,028,471 RGD:8554872
G Zup1 zinc finger containing ubiquitin peptidase 1 JBrowse link 10 33,919,142 33,951,294 RGD:8554872
dopamine beta-hydroxylase deficiency term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dbh dopamine beta hydroxylase JBrowse link 2 27,165,507 27,183,204 RGD:7240710
RGD:8554872
RGD:13592920
G Hspa5 heat shock protein 5 JBrowse link 2 34,772,090 34,776,529 RGD:5685690
neurocirculatory asthenia term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 JBrowse link 8 92,960,470 93,001,667 RGD:1624278
Orthostatic Hypotension term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Abcb1a ATP-binding cassette, sub-family B (MDR/TAP), member 1A JBrowse link 5 8,567,091 8,748,575 RGD:11554173
G Gnas GNAS (guanine nucleotide binding protein, alpha stimulating) complex locus JBrowse link 2 174,284,320 174,346,744 RGD:1580406
G Gnb3 guanine nucleotide binding protein (G protein), beta 3 JBrowse link 6 124,834,240 124,840,275 RGD:1580406
G mt-Nd2 NADH dehydrogenase 2, mitochondrial JBrowse link MT 3,914 4,951 RGD:1581056
G Oprd1 opioid receptor, delta 1 JBrowse link 4 132,110,188 132,144,486 RGD:11554173
G Oprm1 opioid receptor, mu 1 JBrowse link 10 6,758,593 7,038,209 RGD:11554173
Orthostatic Hypotension 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Cyb561 cytochrome b-561 JBrowse link 11 105,933,702 105,945,019 RGD:8554872
RGD:7240710
Orthostatic Intolerance term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 JBrowse link 8 92,960,470 93,001,667 RGD:7240710
RGD:8554872
RGD:11554173
postural orthostatic tachycardia syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Slc6a2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 JBrowse link 8 92,960,470 93,001,667 RGD:13592920
Vasovagal Syncope term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Nppb natriuretic peptide type B JBrowse link 4 147,985,786 147,987,205 RGD:7247623

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13271
    disease of anatomical entity 12755
      nervous system disease 10288
        Neurologic Manifestations 3843
          somatoform disorder 38
            Neurasthenia 0
            body dysmorphic disorder 27
            conversion disorder 0
            hypochondriasis 0
            neurocirculatory asthenia + 11
            pain disorder 0
            somatization disorder 0
Path 2
Term Annotations click to browse term
  disease 13271
    disease of anatomical entity 12755
      nervous system disease 10288
        central nervous system disease 8606
          brain disease 7907
            disease of mental health 5689
              somatoform disorder 38
                Neurasthenia 0
                body dysmorphic disorder 27
                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.