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Details
Link-It Detail - Disease - Congenital hypoplasia of thymus
Debug Stats
  • ### Total Build Time: 30 ms 10.612 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 360 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 7 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 15 bytes
  • CONCEPT_RELATIONSHIPS gt=21 ms Completed: 21 ms rowSize= 2.387 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 6.639 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital hypoplasia of thymus C0685891
Relationships (3)

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


Relationships:
associated_​with : 1
location_​of : 1
used_​for : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATlocation_ofimg Thymus Gland C0040113
DISO_to_DISOassociated_withimg 213 CONGENITAL HYPOPLASIAS C0020636
DISO_to_DISOused_forimg DiGeorge Syndrome C0012236
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanDCLRE1C64421DNA cross-link repair 1C
img OMIM, Score=964, UMLKSK CUI: C0685891
HumanCELF210659CUGBP, Elav-like family member 2
img GENERIF, Score=1000, Pubmed Id: 12110949, UMLKSK CUI: C0685891
HumanTBX16899T-box 1
img OMIM, Score=1000, UMLKSK CUI: C0685891
HumanRAG25897recombination activating gene 2
img OMIM, Score=964, UMLKSK CUI: C0685891
HumanRAG15896recombination activating gene 1
img OMIM, Score=964, UMLKSK CUI: C0685891
HumanIL2RG3561interleukin 2 receptor, gamma
img OMIM, Score=1000, UMLKSK CUI: C0685891
HumanATM472ataxia telangiectasia mutated
img OMIM, Score=1000, UMLKSK CUI: C0685891
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0685891Congenital hypoplasia of thymus0self