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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.


show annotations for term's descendants       view all columns           Sort by:
 
Adams-Oliver syndrome term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G ARHGAP31 Rho GTPase activating protein 31 JBrowse link 3 119,294,289 119,419,476 RGD:8554872
G DLL4 delta like canonical Notch ligand 4 JBrowse link 15 40,929,333 40,939,060 RGD:8554872
RGD:11554173
G DOCK6 dedicator of cytokinesis 6 JBrowse link 19 11,199,293 11,262,501 RGD:11554173
RGD:8554872
G EOGT EGF domain specific O-linked N-acetylglucosamine transferase JBrowse link 3 68,975,212 69,013,961 RGD:8554872
RGD:11554173
G LINC01451 long intergenic non-protein coding RNA 1451 JBrowse link 9 136,612,028 136,617,181 RGD:8554872
G MIR4674 microRNA 4674 JBrowse link 9 136,546,173 136,546,259 RGD:8554872
G NALT1 NOTCH1 associated lncRNA in T cell acute lymphoblastic leukemia 1 JBrowse link 9 136,547,842 136,549,744 RGD:8554872
G NOTCH1 notch receptor 1 JBrowse link 9 136,494,433 136,545,786 RGD:8554872
RGD:11554173
G RBPJ recombination signal binding protein for immunoglobulin kappa J region JBrowse link 4 26,163,489 26,435,131 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 3 119,294,289 119,419,476 RGD:7240710
Adams-Oliver Syndrome 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DOCK6 dedicator of cytokinesis 6 JBrowse link 19 11,199,293 11,262,501 RGD:8554872
RGD:7240710
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 4 26,163,489 26,435,131 RGD:8554872
RGD:7240710
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 3 68,975,212 69,013,961 RGD:8554872
RGD:7240710
Adams-Oliver Syndrome 5 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G LINC01451 long intergenic non-protein coding RNA 1451 JBrowse link 9 136,612,028 136,617,181 RGD:8554872
G MIR4673 microRNA 4673 JBrowse link 9 136,519,568 136,519,626 RGD:8554872
G MIR4674 microRNA 4674 JBrowse link 9 136,546,173 136,546,259 RGD:8554872
G NALT1 NOTCH1 associated lncRNA in T cell acute lymphoblastic leukemia 1 JBrowse link 9 136,547,842 136,549,744 RGD:8554872
G NOTCH1 notch receptor 1 JBrowse link 9 136,494,433 136,545,786 RGD:8554872
RGD:7240710
Adams-Oliver Syndrome 6 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G DLL4 delta like canonical Notch ligand 4 JBrowse link 15 40,929,333 40,939,060 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 10 121,478,330 121,598,458 RGD:8554872
RGD:7240710
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 8 99,013,085 99,877,586 RGD:8554872

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15323
    sensory system disease 4388
      skin disease 2260
        scalp dermatosis 12
          Adams-Oliver syndrome + 10
          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 15323
    disease of anatomical entity 14207
      nervous system disease 10367
        sensory system disease 4388
          skin disease 2260
            scalp dermatosis 12
              Adams-Oliver syndrome + 10
              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