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Details
Link-It Detail - Disease - Acanthosis Nigricans
Debug Stats
  • ### Total Build Time: 177 ms 32.137 KB
  • CONCEPT_NAME gt=10 ms Completed: 10 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 350 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=1 ms Completed: 1 ms rowSize= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=15 ms Completed: 15 ms rowSize= 545 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=39 ms Completed: 39 ms rowSize= 1.505 KB
  • CONCEPT_RELATIONSHIPS gt=91 ms Completed: 91 ms rowSize= 13.741 KB
  • CONCEPT_GENES gt=19 ms Completed: 19 ms rowSize= 14.313 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Acanthosis Nigricans C0000889
Definition (1)
A melanotic cutaneous lesion that develops in the axilla and other body folds. It may be idiopathic, drug-induced, or it may be associated with the presence of an endocrine disorder or malignancy.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Melanosis C0025209
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372746img Melanosis C0025209
Relationships (27)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 1
diso_​to_​diso : 19
diso_​to_​gene : 2
diso_​to_​phen : 2


Relationships:
none : 17
gene_​associated_​with_​disease : 2
is_​associated_​anatomic_​site_​of : 1
is_​finding_​of_​disease : 1
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 1
mapped_​to : 3
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO38img Complication Aspects C1171258
DISO_to_DISO31img Complication Aspects C1171258
DISO_to_PHEN24img genetic aspects C0017399
DISO_to_DISO21img Insulin Resistance C0021655
DISO_to_DISO19img Obesity C0028754
DISO_to_DISO16img Insulin Resistance C0021655
DISO_to_DISO16img Obesity C0028754
DISO_to_CHEM12img Receptor, Fibroblast Growth Factor, Type 3 C0117718
DISO_to_DISO12img Paraneoplastic Syndromes C0030472
DISO_to_PHEN12img genetic aspects C0017399
DISO_to_DISO11img Diabetes Mellitus, Type 2 C0011860
DISO_to_ANAT10img In Blood C0005768
DISO_to_DISO10img Adenocarcinoma C0001418
DISO_to_DISO10img Cutaneous tumor C0037286
DISO_to_DISO8img PARANEOPL SYNDROMES C0030472
DISO_to_DISO7img Abnormalities, Multiple C0000772
DISO_to_DISO7img Hyperandrogenism C0206081
DISO_to_ANATis_associated_anatomic_site_ofimg Integumentary System C0037267
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Skin C1123023
DISO_to_DISOpermuted_term_ofimg Acanthosis Nigricans C0000889
DISO_to_DISOmapped_toimg Acanthosis nigricans muscle cramps acral enlargement C1860215
DISO_to_DISOisaimg Acanthosis nigricans of oral mucous membranes C1304146
DISO_to_DISOis_finding_of_diseaseimg Cutaneous Involvement C1511567
DISO_to_DISOmapped_toimg Familial acanthosis nigricans C2930792
DISO_to_DISOmapped_toimg HAIR-AN syndrome C1963745
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanAGPAT2105551-acylglycerol-3-phosphate O-acyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanALMS17840Alstrom syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanPTEN5728phosphatase and tensin homolog
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanPPP1R3A5506protein phosphatase 1, regulatory subunit 3A
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanPPARG5468peroxisome proliferator-activated receptor gamma
img OMIM, Score=1000, UMLKSK CUI: C0000889
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanLMNA4000lamin A/C
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanKRAS3845Kirsten rat sarcoma viral oncogene homolog
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanINSR3643insulin receptor
img OMIM, Score=1000, UMLKSK CUI: C0000889
img OMIM, Score=1000, UMLKSK CUI: C0000889
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanFGFR22263fibroblast growth factor receptor 2
img OMIM, Score=1000, UMLKSK CUI: C0000889
HumanFGFR32261fibroblast growth factor receptor 3
img GENERIF, Score=694, Pubmed Id: 18000903, UMLKSK CUI: C0000889
img GENERIF, Score=901, Pubmed Id: 17875876, UMLKSK CUI: C0000889
img GENERIF, Score=1000, Pubmed Id: 18583390, UMLKSK CUI: C0000889
img GENERIF, Score=1000, Pubmed Id: 15517832, UMLKSK CUI: C0000889
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0000889Acanthosis Nigricans0self