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Details
Link-It Detail - Disease - Genetic Diseases, Y-Linked
Debug Stats
  • ### Total Build Time: 43 ms 6.648 KB
  • CONCEPT_NAME gt=6 ms Completed: 6 ms rowSize= 405 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 354 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=12 ms Completed: 12 ms rowSize= 560 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.558 KB
  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 2.380 KB
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Genetic Diseases, Y-Linked C1563751
Disease, Y-Linked Genetic
Definition (1)
Genetic diseases that are linked to mutant ALLELES on the Y CHROMOSOME in humans (Y CHROMOSOME, HUMAN) or the Y chromosome in other species. Included here are animal models of human Y-linked diseases.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Genetic Diseases, Inborn C0950123
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501233img Genetic Diseases, Inborn C0950123
Relationships (3)

Relation Types:
diso_​to_​diso : 2
diso_​to_​phen : 1


Relationships:
none : 1
mapped_​to : 1
permuted_​term_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_PHEN4img genetic aspects C0017399
DISO_to_DISOpermuted_term_ofimg Disease, Y-Linked Genetic C1563751
DISO_to_DISOmapped_toimg SERTOLI CELL-ONLY SYNDROME, TYPE I C1839073
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1563751Genetic Diseases, Y-Linked0self