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Details
Link-It Detail - Disease - Penile Diseases
Debug Stats
  • ### Total Build Time: 64 ms 37.965 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 328 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 222 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=4 ms Completed: 4 ms rowSize= 558 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 2.636 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 1.516 KB
  • CONCEPT_RELATIONSHIPS gt=34 ms Completed: 34 ms rowSize= 13.821 KB
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 17.550 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Penile Diseases C0030846
Definition (1)
Pathological processes involving the PENIS or its component tissues.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Genital Diseases, Male C0017412
Children (6)
img Penile Neoplasms C0030849
img Priapism C0033117
img Balanitis C0004690
img Penile Induration C0030848
img Hypospadias C0848558
img Phimosis C0031538
Ancestral Roots
RootRoot Plus OneDepthParent
img Male Urogenital Diseases C1720894img Genital Diseases, Male C00174123img Genital Diseases, Male C0017412
Relationships (102)

Relation Types:
diso_​to_​anat : 9
diso_​to_​diso : 92
diso_​to_​phys : 1


Relationships:
none : 43
associated_​with : 1
classifies : 1
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 2
isa : 40
location_​of : 1
mapped_​to : 10
related_​to : 3
Page Size
Current 25
  Page 1 of 5
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT111img Penis C0030851
DISO_to_ANAT61img Penis C0030851
DISO_to_DISO26img Complication Aspects C1171258
DISO_to_DISO24img chemically induced C0007994
DISO_to_DISO23img chemically induced C0007994
DISO_to_DISO22img Complication Aspects C1171258
DISO_to_ANAT21img Scrotum C0036471
DISO_to_DISO20img Condylomata Acuminata C0009663
DISO_to_ANAT16img Scrotum C0036471
DISO_to_DISO16img Condylomata Acuminata C0009663
DISO_to_DISO15img LICHEN SCLEROSUS ET ATROPHICUS C0023652
DISO_to_DISO14img LICHEN SCLEROSUS ET ATROPHICUS C0023652
DISO_to_DISO13img Dermatologic disorders C0037274
DISO_to_DISO13img Disease due to Papilloma virus C0950124
DISO_to_DISO13img Skin Ulcer C0037299
DISO_to_DISO10img Crohn Disease C0010346
DISO_to_DISO10img Cyst C0010709
DISO_to_DISO10img Granuloma C0018188
DISO_to_DISO10img Ulcer C0041582
DISO_to_ANAT9img Surgical Flaps C0038925
DISO_to_DISO9img Calciphylaxes C0006666
DISO_to_DISO9img Dermatologic disorders C0037274
DISO_to_DISO9img Disease due to Papilloma virus C0950124
DISO_to_DISO9img Edema C0013604
DISO_to_DISO9img Erectile Dysfunction C0242350
Genes (78)

Species:
human : 78
Page Size
Current 25
  Page 1 of 4
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanHYLS1219844hydrolethalus syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanFRAS180144Fraser syndrome 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanPEX2655670peroxisomal biogenesis factor 26
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanFERMT155612fermitin family member 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanZMPSTE2410269zinc metallopeptidase STE24
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanPQBP110084polyglutamine binding protein 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanMAMLD110046mastermind-like domain containing 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanZEB29839zinc finger E-box binding homeobox 2
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanCUL79820cullin 7
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanWTAP9589Wilms tumor 1 associated protein
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanTP638626tumor protein p63
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanPEX38504peroxisomal biogenesis factor 3
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanCUL4B8450cullin 4B
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanWT17490Wilms tumor 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanWNT7A7476wingless-type MMTV integration site family, member 7A
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanTGFB17040transforming growth factor, beta 1
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanHNF1B6928HNF1 homeobox B
INFERRED, Score=800, UMLKSK CUI: C0030846
HumanSTAR6770steroidogenic acute regulatory protein
INFERRED, Score=800, UMLKSK CUI: C0030846
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0030846Penile Diseases0self