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Details
Link-It Detail - Disease - Melanosis
Debug Stats
  • ### Total Build Time: 53 ms 29.949 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 316 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 250 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=0 Completed: 0 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=5 ms Completed: 5 ms rowSize= 553 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 983 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 1.513 KB
  • CONCEPT_RELATIONSHIPS gt=17 ms Completed: 17 ms rowSize= 12.802 KB
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 12.228 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.144 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Melanosis C0025209
Definition (1)
Disorders of increased melanin pigmentation that develop without preceding inflammatory disease.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Hyperpigmentation C0162834
Children (2)
img Acanthosis Nigricans C0000889
img Lentigo C0023321
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372745img Hyperpigmentation C0162834
Relationships (55)

Relation Types:
diso_​to_​anat : 2
diso_​to_​chem : 12
diso_​to_​diso : 39
diso_​to_​phen : 2


Relationships:
none : 36
associated_​with : 1
isa : 11
mapped_​to : 6
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO52img Complication Aspects C1171258
DISO_to_DISO50img Melanoma C0025202
DISO_to_DISO49img Complication Aspects C1171258
DISO_to_DISO44img Melanoma C0025202
DISO_to_DISO44img Neurocutaneous Syndromes C0265316
DISO_to_DISO42img Neurocutaneous Syndromes C0265316
DISO_to_DISO37img Cutaneous tumor C0037286
DISO_to_DISO33img Melanocytic nevus C0027962
DISO_to_DISO28img Cutaneous tumor C0037286
DISO_to_DISO28img chemically induced C0007994
DISO_to_DISO26img Dermatoses, Facial C0015456
DISO_to_CHEM25img AGENT DERMATOL C0011625
DISO_to_CHEM22img DIHYDROXYBENZENES P C0020307
DISO_to_DISO21img Melanocytic nevus C0027962
DISO_to_PHEN21img genetic aspects C0017399
DISO_to_CHEM17img Tretinoin C0040845
DISO_to_ANAT16img Melanocytes C0025201
DISO_to_ANAT15img Skin C1123023
DISO_to_CHEM15img DIHYDROXYBENZENES P C0020307
DISO_to_DISO15img CONJUNCTIVAL NEOPL C0009761
DISO_to_DISO15img chemically induced C0007994
DISO_to_CHEM14img AGENT DERMATOL C0011625
DISO_to_DISO13img CONJUNCTIVAL NEOPL C0009761
DISO_to_DISO13img Dermatoses, Facial C0015456
DISO_to_PHEN13img genetic aspects C0017399
Genes (20)

Species:
human : 20
SpeciesGeneGeneIdGene NameEvidence
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanALMS17840Alstrom syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanTYR7299tyrosinase
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanTSC27249tuberous sclerosis 2
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanSTK116794serine/threonine kinase 11
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanRAF15894v-raf-1 murine leukemia viral oncogene homolog 1
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanPTPN115781protein tyrosine phosphatase, non-receptor type 11
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanPTEN5728phosphatase and tensin homolog
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanPRKAR1A5573protein kinase, cAMP-dependent, regulatory, type I, alpha
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanPPP1R3A5506protein phosphatase 1, regulatory subunit 3A
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanPPARG5468peroxisome proliferator-activated receptor gamma
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanMITF4286microphthalmia-associated transcription factor
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanMC1R4157melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanLMNA4000lamin A/C
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanKRAS3845Kirsten rat sarcoma viral oncogene homolog
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanINSR3643insulin receptor
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanFGFR22263fibroblast growth factor receptor 2
INFERRED, Score=800, UMLKSK CUI: C0025209
HumanFGFR32261fibroblast growth factor receptor 3
INFERRED, Score=800, UMLKSK CUI: C0025209
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0025209Melanosis0self