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Details
Link-It Detail - Disease - Gonadal Disorders
Debug Stats
  • ### Total Build Time: 49 ms 33.908 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 332 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 318 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=0 Completed: 0 ms rowSize= 561 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.113 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.119 KB
  • CONCEPT_RELATIONSHIPS gt=4 ms Completed: 4 ms rowSize= 8.634 KB
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 18.497 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.151 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Gonadal Disorders C0018050
Definition (1)
condition in which there is a deviation from or interruption of the normal structure or function of the gamete producing organs; specific gonad disorders available.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Endocrine System Diseases C0014130
Children (7)
img Disorders of Sex Development C0036875
img Testicular Diseases C0039584
img Hypogonadism C0020619
img Puberty, Delayed C0034012
img Female Athlete Triad Syndrome C1721053
img Ovarian Diseases C0029928
img Puberty, Precocious C0034013
Ancestral Roots
RootRoot Plus OneDepthParent
img Endocrine System Diseases C00141302img Endocrine System Diseases C0014130
Relationships (19)

Relation Types:
diso_​to_​anat : 4
diso_​to_​chem : 2
diso_​to_​diso : 10
diso_​to_​phen : 2
diso_​to_​phys : 1


Relationships:
none : 12
is_​associated_​anatomic_​site_​of : 2
isa : 4
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN6img genetic aspects C0017399
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_CHEM4img Antineoplastic Agents C0003392
DISO_to_DISO4img Complication Aspects C1171258
DISO_to_DISO4img chemically induced C0007994
DISO_to_ANAT3img Gonadal structure C0018067
DISO_to_ANAT3img In Blood C0005768
DISO_to_CHEM3img INHIBIN C0021463
DISO_to_DISO3img Hodgkin Disease C0019829
DISO_to_DISO3img Infertility C0021359
DISO_to_DISO3img Neoplasms C0027651
DISO_to_PHYS3img Puberty C0034011
DISO_to_ANATis_associated_anatomic_site_ofimg Gonadal structure C0018067
DISO_to_ANATis_associated_anatomic_site_ofimg Reproductive system C1261210
DISO_to_DISOpermuted_term_ofimg Disease of gonad C0018050
DISO_to_DISOisaimg Germ Cell Neoplasm of Testis C1336708
DISO_to_DISOisaimg Non-Neoplastic Gonadal Disorder C1335012
DISO_to_DISOisaimg Ovarian Germ Cell Tumor C0238324
DISO_to_DISOisaimg Reproductive Endocrine Neoplasm C1335756
Genes (667)

Species:
human : 667
Page Size
Current 25
  Page 1 of 27
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanGGT2728441gamma-glutamyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanPALM2-AKAP2445815
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanLHX8431707LIM homeobox 8
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanNANOS3342977nanos homolog 3 (Drosophila)
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanFREM2341640FRAS1 related extracellular matrix protein 2
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanRSPO1284654R-spondin 1
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanMAGEA2B266740melanoma antigen family A, 2B
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanBRWD3254065bromodomain and WD repeat domain containing 3
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanBBS12166379Bardet-Biedl syndrome 12
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanKLB152831klotho beta
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanSIX5147912SIX homeobox 5
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanSERPINA12145264serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 12
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanE2F7144455E2F transcription factor 7
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanNOBOX135935NOBOX oogenesis homeobox
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanEVC2132884Ellis van Creveld syndrome 2
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanBBS5129880Bardet-Biedl syndrome 5
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanPROKR2128674prokineticin receptor 2
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanNLRP5126206NLR family, pyrin domain containing 5
INFERRED, Score=800, UMLKSK CUI: C0018050
HumanOVCA2124641ovarian tumor suppressor candidate 2
INFERRED, Score=800, UMLKSK CUI: C0018050
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0018050Gonadal Disorders0self