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ONTOLOGY REPORT - ANNOTATIONS


Term:scalp dermatosis
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Accession:DOID:3136 term browser browse the term
Definition:Skin diseases involving the SCALP.
Synonyms:exact_synonym: dermatosis of scalp;   scalp dermatoses
 primary_id: MESH:D012536
 alt_id: RDO:0000833
For additional species annotation, visit the Alliance of Genome Resources.


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Adams-Oliver syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ARHGAP31 Rho GTPase activating protein 31 JBrowse link 33 22,965,941 23,079,590 RGD:9068941
G DLL4 delta like canonical Notch ligand 4 JBrowse link 30 8,059,463 8,068,742 RGD:9068941
G DOCK6 dedicator of cytokinesis 6 JBrowse link 20 50,029,354 50,066,829 RGD:9068941
G EOGT EGF domain specific O-linked N-acetylglucosamine transferase JBrowse link 20 22,722,142 22,757,188 RGD:9068941
G NOTCH1 notch receptor 1 JBrowse link 9 48,975,972 49,018,985 RGD:9068941
G RBPJ recombination signal binding protein for immunoglobulin kappa J region JBrowse link 3 84,060,417 84,286,008 RGD:9068941
Adams-Oliver Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ARHGAP31 Rho GTPase activating protein 31 JBrowse link 33 22,965,941 23,079,590 RGD:7240710
Adams-Oliver Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DOCK6 dedicator of cytokinesis 6 JBrowse link 20 50,029,354 50,066,829 RGD:7240710
RGD:9068941
Adams-Oliver Syndrome 3 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G RBPJ recombination signal binding protein for immunoglobulin kappa J region JBrowse link 3 84,060,417 84,286,008 RGD:7240710
RGD:9068941
Adams-Oliver Syndrome 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G EOGT EGF domain specific O-linked N-acetylglucosamine transferase JBrowse link 20 22,722,142 22,757,188 RGD:7240710
RGD:9068941
Adams-Oliver Syndrome 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G NOTCH1 notch receptor 1 JBrowse link 9 48,975,972 49,018,985 RGD:7240710
RGD:9068941
Adams-Oliver Syndrome 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DLL4 delta like canonical Notch ligand 4 JBrowse link 30 8,059,463 8,068,742 RGD:7240710
RGD:9068941
Beare-Stevenson cutis gyrata syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G FGFR2 fibroblast growth factor receptor 2 JBrowse link 28 31,303,882 31,411,015 RGD:7240710
RGD:9068941
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G VPS13B vacuolar protein sorting 13 homolog B JBrowse link 13 1,101,226 1,834,933 RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11199
    sensory system disease 3910
      skin disease 2051
        scalp dermatosis 8
          Adams-Oliver syndrome + 6
          Akesson Syndrome 0
          Beare-Stevenson cutis gyrata syndrome 1
          Cutis Verticis Gyrata and Mental Deficiency 0
          Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 1
          Dandruff 0
          Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 0
          Rosenthal-Kloepfer Syndrome 0
          tinea capitis + 0
Path 2
Term Annotations click to browse term
  disease 11199
    disease of anatomical entity 10750
      nervous system disease 8289
        sensory system disease 3910
          skin disease 2051
            scalp dermatosis 8
              Adams-Oliver syndrome + 6
              Akesson Syndrome 0
              Beare-Stevenson cutis gyrata syndrome 1
              Cutis Verticis Gyrata and Mental Deficiency 0
              Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness 1
              Dandruff 0
              Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 0
              Rosenthal-Kloepfer Syndrome 0
              tinea capitis + 0
paths to the root