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Details
Link-It Detail - Disease - Cryptorchidism
Debug Stats
  • ### Total Build Time: 189 ms 49.673 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 326 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 480 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= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=7 ms Completed: 7 ms rowSize= 997 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=13 ms Completed: 13 ms rowSize= 6.714 KB
  • CONCEPT_RELATIONSHIPS gt=114 ms Completed: 114 ms rowSize= 13.914 KB
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 25.914 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.148 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Cryptorchidism C0010417
Definition (1)
A developmental defect in which a TESTIS or both TESTES failed to descend from high in the ABDOMEN to the bottom of the SCROTUM. Testicular descent is essential to normal SPERMATOGENESIS which requires temperature lower than the BODY TEMPERATURE. Cryptorchidism can be subclassified by the location of the maldescended testis.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (2)
img Urogenital Abnormalities C0042063
img Testicular Diseases C0039584
Ancestral Roots
RootRoot Plus OneDepthParent
img Male Urogenital Diseases C1720894img Urogenital Abnormalities C00420633img Urogenital Abnormalities C0042063
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Urogenital Abnormalities C0042063
img Female Urogenital Diseases and Pregnancy Complications C1720765img Female Urogenital Diseases C17208874img Urogenital Abnormalities C0042063
img Male Urogenital Diseases C1720894img Genital Diseases, Male C00174124img Testicular Diseases C0039584
img Endocrine System Diseases C0014130img Gonadal Disorders C00180504img Testicular Diseases C0039584
Relationships (77)

Relation Types:
diso_​to_​anat : 16
diso_​to_​chem : 5
diso_​to_​diso : 51
diso_​to_​phen : 2
diso_​to_​phys : 3


Relationships:
none : 46
alias_​of : 1
associated_​with : 7
classified_​as : 2
classifies : 1
is_​associated_​anatomic_​site_​of : 2
isa : 1
location_​of : 1
mapped_​to : 16
Page Size
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Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANAT166img Testis C0039597
DISO_to_ANAT134img Testis C0039597
DISO_to_DISO103img Complication Aspects C1171258
DISO_to_DISO95img Complication Aspects C1171258
DISO_to_PHEN90img genetic aspects C0017399
DISO_to_PHEN53img genetic aspects C0017399
DISO_to_DISO47img Testicular Neoplasms C0039590
DISO_to_DISO38img Hypospadias C0848558
DISO_to_DISO38img Infertility, Male C0021364
DISO_to_DISO32img chemically induced C0007994
DISO_to_DISO27img HERNIA, INGUINAL C0019294
DISO_to_PHYS26img Apoptosis C0162638
DISO_to_ANAT25img Scrotum C0036471
DISO_to_DISO23img Infertility, Male C0021364
DISO_to_ANAT21img In Blood C0005768
DISO_to_ANAT19img In Blood C0005768
DISO_to_DISO19img Abnormalities, Multiple C0000772
DISO_to_CHEM18img Chorionic Gonadotropin C0018062
DISO_to_DISO17img chemically induced C0007994
DISO_to_ANAT16img Spermatozoa C0037868
DISO_to_ANAT15img Epididymis C0014533
DISO_to_DISO15img HERNIA, INGUINAL C0019294
DISO_to_PHYS15img Spermatogenesis C0037864
DISO_to_ANAT14img Inguinal Canal C0021445
DISO_to_CHEM14img Proteins C0033684
Genes (96)

Species:
human : 96
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanBRWD3254065bromodomain and WD repeat domain containing 3
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanESCO2157570establishment of sister chromatid cohesion N-acetyltransferase 2
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanEVC2132884Ellis van Creveld syndrome 2
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanDNAJC19131118DnaJ (Hsp40) homolog, subfamily C, member 19
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanRXFP2122042relaxin/insulin-like family peptide receptor 2
img GENERIF, Score=1000, Pubmed Id: 14656401, UMLKSK CUI: C0010417
img GENERIF, Score=1000, Pubmed Id: 18772597, UMLKSK CUI: C0010417
img GENERIF, Score=1000, Pubmed Id: 18073304, UMLKSK CUI: C0010417
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanPHF684295PHD finger protein 6
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanFRAS180144Fraser syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanPORCN64840porcupine homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanSTRA664220stimulated by retinoic acid 6
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanPEX2655670peroxisomal biogenesis factor 26
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanCHD755636chromodomain helicase DNA binding protein 7
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanRAB2351715RAB23, member RAS oncogene family
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanNIPBL25836Nipped-B homolog (Drosophila)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanRAB3GAP225782RAB3 GTPase activating protein subunit 2 (non-catalytic)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanRAB3GAP122930RAB3 GTPase activating protein subunit 1 (catalytic)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanKCNQ1OT110984KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanSEC23A10484Sec23 homolog A (S. cerevisiae)
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanCD9610225CD96 molecule
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanZEB29839zinc finger E-box binding homeobox 2
img OMIM, Score=1000, UMLKSK CUI: C0010417
HumanSEMA3E9723sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
img OMIM, Score=1000, UMLKSK CUI: C0010417
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0010417Cryptorchidism0self