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Details
Link-It Detail - Disease - Hypertrichosis
Debug Stats
  • ### Total Build Time: 267 ms 36.396 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 300 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= 240 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=9 ms Completed: 9 ms rowSize= 549 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 1.509 KB
  • CONCEPT_RELATIONSHIPS gt=203 ms Completed: 203 ms rowSize= 13.119 KB
  • CONCEPT_GENES gt=34 ms Completed: 34 ms rowSize= 19.203 KB
  • CONCEPT_XREFS gt=4 ms Completed: 4 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hypertrichosis C0020555
Definition (1)
A disorder characterized by hair density or length beyond the accepted limits of normal in a particular body region, for a particular age or race.
Semantic Types (2)
Disease or Syndrome (T047)
Sign or Symptom (T184)
Parents (1)
img Hair Diseases C0018500
Ancestral Roots
RootRoot Plus OneDepthParent
img Skin and Connective Tissue Diseases C0175166img Skin Diseases C00372744img Hair Diseases C0018500
Relationships (61)

Relation Types:
diso_​to_​anat : 3
diso_​to_​chem : 10
diso_​to_​diso : 46
diso_​to_​phen : 2


Relationships:
none : 19
isa : 16
location_​of : 1
mapped_​to : 20
may_​treat : 4
permuted_​term_​of : 1
Page Size
Current 25
  Page 1 of 3
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO35img chemically induced C0007994
DISO_to_PHEN26img genetic aspects C0017399
DISO_to_DISO22img Complication Aspects C1171258
DISO_to_DISO20img chemically induced C0007994
DISO_to_ANAT17img Eyelash C0015422
DISO_to_PHEN17img genetic aspects C0017399
DISO_to_ANAT14img Eyelash C0015422
DISO_to_DISO13img Abnormalities, Multiple C0000772
DISO_to_DISO13img Complication Aspects C1171258
DISO_to_CHEM12img Quinazoline C0034407
DISO_to_CHEM10img Antineoplastic Agents C0003392
DISO_to_DISO10img Hyperpigmentation C0162834
DISO_to_CHEM8img Antihypertensive Agents C0003364
DISO_to_DISO8img Lung Neoplasms C0024121
DISO_to_CHEM7img Antibodies, Monoclonal C0003250
DISO_to_CHEM7img Epidermal Growth Factor Receptor C0034802
DISO_to_CHEM7img Protein Kinase Inhibitors C1449702
DISO_to_DISO7img Abnormalities, Multiple C0000772
DISO_to_DISO7img Adenocarcinoma C0001418
DISO_to_ANATlocation_ofimg Hair C0018494
DISO_to_CHEMmay_treatimg 2-(Difluoromethyl)-dl-ornithine Hydrochloride, Monohydrate C0282042
DISO_to_CHEMmay_treatimg EFLORNITHINE HCL 13.9 % TOPICAL CREAM (GRAMS) C0981426
DISO_to_CHEMmay_treatimg EFLORNITHINE HCL 200MG/ML INJ C0976585
DISO_to_CHEMmay_treatimg Eflornithine C0002260
DISO_to_DISOmapped_toimg AFA SYNDROME C0796280
Genes (21)

Species:
human : 21
SpeciesGeneGeneIdGene NameEvidence
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanC8orf38137682
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanSOX1854345SRY (sex determining region Y)-box 18
img GENERIF, Score=660, Pubmed Id: 12740761, UMLKSK CUI: C0020555
HumanFST10468follistatin
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanUROS7390uroporphyrinogen III synthase
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanTRPS17227trichorhinophalangeal syndrome I
img GENERIF, Score=1000, Pubmed Id: 18713754, UMLKSK CUI: C0020555
HumanSURF16834surfeit 1
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanSDHA6389succinate dehydrogenase complex, subunit A, flavoprotein (Fp)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanNDUFS84728NADH dehydrogenase (ubiquinone) Fe-S protein 8, 23kDa (NADH-coenzyme Q reductase)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanNDUFS44724NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanNDUFV14723NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanNDUFS34722NADH dehydrogenase (ubiquinone) Fe-S protein 3, 30kDa (NADH-coenzyme Q reductase)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanNDUFA24695NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 2, 8kDa
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanMMP24313matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanINSR3643insulin receptor
img OMIM, Score=1000, UMLKSK CUI: C0020555
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanGLB12720galactosidase, beta 1
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanDLD1738dihydrolipoamide dehydrogenase
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanCOX151355cytochrome c oxidase assembly homolog 15 (yeast)
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanBLM641Bloom syndrome, RecQ helicase-like
img OMIM, Score=1000, UMLKSK CUI: C0020555
HumanBCS1L617BC1 (ubiquinol-cytochrome c reductase) synthesis-like
img OMIM, Score=1000, UMLKSK CUI: C0020555
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020555Hypertrichosis0self