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Details
Link-It Detail - Disease - Porokeratosis
Debug Stats
  • ### Total Build Time: 105 ms 21.761 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 324 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 346 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=4 ms Completed: 4 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=6 ms Completed: 6 ms rowSize= 985 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 4.110 KB
  • CONCEPT_RELATIONSHIPS gt=65 ms Completed: 65 ms rowSize= 13.300 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 1.368 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Porokeratosis C0162839
Definition (1)
A clonal proliferation of abnormal keratinocytes characterized by the development of localized or multiple atrophic skin patches surrounded by an annular keratotic ring called cornoid lamella.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Keratosis C0022593
img Skin Diseases, Genetic C0037277
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Keratosis C0022593
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Skin Diseases, Genetic C0037277
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501234img Skin Diseases, Genetic C0037277
Relationships (30)

Relation Types:
diso_​to_​anat : 5
diso_​to_​chem : 2
diso_​to_​diso : 21
diso_​to_​phen : 2


Relationships:
none : 15
associated_​with : 3
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 5
mapped_​to : 4
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO28img Complication Aspects C1171258
DISO_to_DISO19img Complication Aspects C1171258
DISO_to_DISO16img Cutaneous tumor C0037286
DISO_to_PHEN16img genetic aspects C0017399
DISO_to_PHEN15img genetic aspects C0017399
DISO_to_DISO13img Cutaneous tumor C0037286
DISO_to_ANAT12img Skin C1123023
DISO_to_DISO9img Cellular naevus C0206737
DISO_to_CHEM7img Aminoquinolines C0002588
DISO_to_DISO7img Sweat Gland Neoplasms C0038987
DISO_to_ANAT6img Buttocks C0006497
DISO_to_ANAT6img Scrotum C0036471
DISO_to_CHEM6img Adjuvants, Immunologic C0001551
DISO_to_DISO6img Carcinoma, Squamous Cell C0007137
DISO_to_DISO6img Dermatoses, Leg C0023219
DISO_to_ANATis_associated_anatomic_site_ofimg Integumentary System C0037267
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skin C1123023
DISO_to_DISOmapped_toimg CDAGS SYNDROME C1864186
DISO_to_DISOassociated_withimg Congenital Abnormalities C0000768
DISO_to_DISOmapped_toimg Congenital facial linear porokeratosis C2931908
DISO_to_DISOis_finding_of_diseaseimg Cutaneous Involvement C1511567
DISO_to_DISOisaimg Disseminated superficial porokeratosis C0406347
DISO_to_DISOassociated_withimg Hyperkeratosis C0870082
DISO_to_DISOmapped_toimg KERATODERMA, PALMOPLANTAR, PUNCTATE TYPE II C1867982
DISO_to_DISOisaimg Keratoderma Palmoplantar, Punctate Type 2 C0162838
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanSART39733squamous cell carcinoma antigen recognized by T cells 3
img OMIM, Score=833, UMLKSK CUI: C0162839
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0162839Porokeratosis0self