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Details
Link-It Detail - Disease - Lentigo
Debug Stats
  • ### Total Build Time: 180 ms 26.394 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 312 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 466 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=3 ms Completed: 3 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 545 bytes
  • CONCEPT_CHILDREN gt=7 ms Completed: 7 ms rowSize= 994 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=22 ms Completed: 22 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=113 ms Completed: 113 ms rowSize= 12.963 KB
  • CONCEPT_GENES gt=15 ms Completed: 15 ms rowSize= 8.311 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.142 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Lentigo C0023321
Definition (1)
Small circumscribed melanoses resembling, but differing histologically from, freckles. The concept includes senile lentigo ('liver spots') and nevoid lentigo (nevus spilus, lentigo simplex) and may also occur in association with multiple congenital defects or congenital syndromes (e.g., Peutz-Jeghers syndrome).
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Melanosis C0025209
Children (2)
img LEOPARD Syndrome C0175704
img Peutz-Jeghers Syndrome C0031269
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372746img Melanosis C0025209
Relationships (38)

Relation Types:
diso_​to_​anat : 4
diso_​to_​diso : 29
diso_​to_​phen : 4
diso_​to_​phys : 1


Relationships:
none : 19
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 1
isa : 14
location_​of : 1
mapped_​to : 1
used_​for : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO29img Cutaneous tumor C0037286
DISO_to_DISO19img Cutaneous tumor C0037286
DISO_to_DISO18img Complication Aspects C1171258
DISO_to_PHEN15img genetic aspects C0017399
DISO_to_PHEN14img genetic aspects C0017399
DISO_to_DISO13img Melanoma C0025202
DISO_to_DISO10img Melanoma C0025202
DISO_to_DISO8img Complication Aspects C1171258
DISO_to_DISO8img Nevus, Pigmented C0027962
DISO_to_PHEN8img Sunlight C0038817
DISO_to_ANAT7img Skin C1123023
DISO_to_DISO7img Melanocytic nevus C0027962
DISO_to_PHYS7img Aging Skin C0037271
DISO_to_ANAT6img Melanocytes C0025201
DISO_to_DISO6img Facial Dermatoses C0015456
DISO_to_DISO6img Melanosis C0025209
DISO_to_DISO6img Nevus C0027960
DISO_to_DISO6img chemically induced C0007994
DISO_to_PHEN6img Sunlight C0038817
DISO_to_ANATis_associated_anatomic_site_ofimg Integumentary System C0037267
DISO_to_ANATlocation_ofimg Skin C1123023
DISO_to_DISOisaimg Acquired lentiginosis C0456992
DISO_to_DISOisaimg Actinic lentigo C0036651
DISO_to_DISOisaimg Cardiomyopathic, Lentiginosis C0175704
DISO_to_DISOisaimg Carney Complex C0406810
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanTYR7299tyrosinase
img OMIM, Score=1000, UMLKSK CUI: C0023321
HumanTSC27249tuberous sclerosis 2
INFERRED, Score=800, UMLKSK CUI: C0023321
HumanSTK116794serine/threonine kinase 11
INFERRED, Score=800, UMLKSK CUI: C0023321
HumanRAF15894v-raf-1 murine leukemia viral oncogene homolog 1
INFERRED, Score=800, UMLKSK CUI: C0023321
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
img OMIM, Score=770, UMLKSK CUI: C0023321
img OMIM, Score=1000, UMLKSK CUI: C0023321
img OMIM, Score=1000, UMLKSK CUI: C0023321
img OMIM, Score=1000, UMLKSK CUI: C0023321
HumanPRKAR1A5573protein kinase, cAMP-dependent, regulatory, type I, alpha
img OMIM, Score=833, UMLKSK CUI: C0023321
HumanMITF4286microphthalmia-associated transcription factor
img OMIM, Score=1000, UMLKSK CUI: C0023321
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
img GENERIF, Score=861, Pubmed Id: 18079748, UMLKSK CUI: C0023321
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023321Lentigo0self