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Details
Link-It Detail - Disease - Gingival Diseases
Debug Stats
  • ### Total Build Time: 255 ms 37.487 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 274 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=2 ms Completed: 2 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 556 bytes
  • CONCEPT_CHILDREN gt=92 ms Completed: 92 ms rowSize= 3.093 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=116 ms Completed: 116 ms rowSize= 12.980 KB
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 17.412 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gingival Diseases C0017563
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the gums or gingiva.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Periodontal Diseases C0031090
Children (7)
img Gingival Overgrowth C0376480
img Granuloma, Giant Cell C0018194
img Gingival Recession C0017572
img Gingivitis C0017574
img Pericoronitis C0031055
img Gingival Hemorrhage C0017565
img Gingival Neoplasms C0017570
Ancestral Roots
RootRoot Plus OneDepthParent
img Stomatognathic Diseases C0038368img Mouth Diseases C00266364img Periodontal Diseases C0031090
Relationships (67)

Relation Types:
diso_​to_​anat : 6
diso_​to_​chem : 2
diso_​to_​diso : 59


Relationships:
none : 27
associated_​with : 1
entry_​version_​of : 1
isa : 34
location_​of : 1
mapped_​to : 1
related_​to : 2
Page Size
Current 25
  Page 1 of 3
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Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO22img Giant Cell Granuloma C0018194
DISO_to_DISO21img Granuloma, Pyogenic C0085653
DISO_to_DISO21img chemically induced C0007994
DISO_to_ANAT20img Gingiva C0017562
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO18img Pigmentation Disorders C0549567
DISO_to_ANAT16img Gingiva C0017562
DISO_to_DISO16img Complication Aspects C1171258
DISO_to_DISO13img Benign Mucosal Pemphigoid C0030804
DISO_to_ANAT11img Mouth Mucosa C0026639
DISO_to_DISO11img GINGIVAL NEOPL C0017570
DISO_to_DISO11img Giant Cell Granuloma C0018194
DISO_to_DISO10img Granuloma, Pyogenic C0085653
DISO_to_DISO10img Lichen Planus, Oral C0206139
DISO_to_DISO10img chemically induced C0007994
DISO_to_CHEM9img ALLOY, AMALGAM C0011324
DISO_to_CHEM9img Dental Amalgam C0011324
DISO_to_DISO8img Hyperpigmentation C0162834
DISO_to_DISO8img Melanosis C0025209
DISO_to_DISO8img Oral Ulcer C0149745
DISO_to_DISO8img Pigmentation Disorders C0549567
DISO_to_ANAT7img Mouth Mucosa C0026639
DISO_to_ANAT7img Palate C0700374
DISO_to_DISO7img Benign Mucosal Pemphigoid C0030804
DISO_to_DISO7img GINGIVAL NEOPL C0017570
Genes (57)

Species:
human : 57
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBLOC1S3388552biogenesis of lysosomal organelles complex-1, subunit 3
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanANTXR2118429anthrax toxin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanHPS489781Hermansky-Pudlak syndrome 4
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanHPS384343Hermansky-Pudlak syndrome 3
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanDTNBP184062dystrobrevin binding protein 1
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanHPS679803Hermansky-Pudlak syndrome 6
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanGINGF264644gingival fibromatosis, hereditary, 2
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanFAM20C56975family with sequence similarity 20, member C
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSAMD954809sterile alpha motif domain containing 9
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSLC17A526503solute carrier family 17 (acidic sugar transporter), member 5
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanHPS511234Hermansky-Pudlak syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanADAMTS29509ADAM metallopeptidase with thrombospondin type 1 motif, 2
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSMC39126structural maintenance of chromosomes 3
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanTNFRSF11A8792tumor necrosis factor receptor superfamily, member 11a, NFKB activator
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanALMS17840Alstrom syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanTNF7124tumor necrosis factor
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanTLR27097toll-like receptor 2
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanTERT7015telomerase reverse transcriptase
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSPARC6678secreted protein, acidic, cysteine-rich (osteonectin)
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSOS16654son of sevenless homolog 1 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanSH3BP26452SH3-domain binding protein 2
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanS100A96280S100 calcium binding protein A9
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanMAPK105602mitogen-activated protein kinase 10
INFERRED, Score=800, UMLKSK CUI: C0017563
HumanPLG5340plasminogen
INFERRED, Score=800, UMLKSK CUI: C0017563
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0017563Gingival Diseases0self