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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 16 38,598,343 38,713,035 RGD:8554872
RGD:11554173
G Dll4 delta like canonical Notch ligand 4 JBrowse link 2 119,325,784 119,335,666 RGD:8554872
RGD:11554173
G Dock6 dedicator of cytokinesis 6 JBrowse link 9 21,800,180 21,852,716 RGD:11554173
RGD:8554872
G Eogt EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase JBrowse link 6 97,110,016 97,149,703 RGD:8554872
RGD:11554173
G Notch1 notch 1 JBrowse link 2 26,457,902 26,503,822 RGD:11554173
G Rbpj recombination signal binding protein for immunoglobulin kappa J region JBrowse link 5 53,466,115 53,657,445 RGD:11554173
Adams-Oliver Syndrome 1 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Arhgap31 Rho GTPase activating protein 31 JBrowse link 16 38,598,343 38,713,035 RGD:7240710
RGD:8554872
G Notch1 notch 1 JBrowse link 2 26,457,902 26,503,822 RGD:8554872
Adams-Oliver Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dock6 dedicator of cytokinesis 6 JBrowse link 9 21,800,180 21,852,716 RGD:7240710
RGD:8554872
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 5 53,466,115 53,657,445 RGD:7240710
RGD:8554872
Adams-Oliver Syndrome 4 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Eogt EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase JBrowse link 6 97,110,016 97,149,703 RGD:7240710
RGD:8554872
Adams-Oliver Syndrome 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Notch1 notch 1 JBrowse link 2 26,457,902 26,503,822 RGD:7240710
RGD:8554872
Adams-Oliver Syndrome 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Dll4 delta like canonical Notch ligand 4 JBrowse link 2 119,325,784 119,335,666 RGD:8554872
RGD:7240710
Beare-Stevenson cutis gyrata syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Fgfr2 fibroblast growth factor receptor 2 JBrowse link 7 130,162,451 130,266,944 RGD:7240710
RGD:8554872
RGD:13592920
Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Vps13b vacuolar protein sorting 13B JBrowse link 15 35,371,143 35,931,229 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 11667
    sensory system disease 4005
      skin disease 2108
        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 11667
    disease of anatomical entity 11172
      nervous system disease 8510
        sensory system disease 4005
          skin disease 2108
            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