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Details
Link-It Detail - Disease - Congenital absence of spleen
Debug Stats
  • ### Total Build Time: 13 ms 10.625 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 354 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=1 ms Completed: 1 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=4 ms Completed: 4 ms rowSize= 2.715 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 6.332 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.162 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Congenital absence of spleen C0600031
Relationships (4)

Relation Types:
diso_​to_​anat : 1
diso_​to_​diso : 3


Relationships:
associated_​with : 1
isa : 2
location_​of : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATlocation_ofimg Spleen C0037993
DISO_to_DISOisaimg ASPLENIA WITH CARDIOVASCULAR ANOMALIES C0175707
DISO_to_DISOassociated_withimg Congenital absence C0332907
DISO_to_DISOisaimg Functional asplenia C0272405
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanMKS154903Meckel syndrome, type 1
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanNPHP327031nephronophthisis 3 (adolescent)
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanDNAI127019dynein, axonemal, intermediate chain 1
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanZIC37547Zic family member 3
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanWNT37473wingless-type MMTV integration site family, member 3
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanMYCN4613v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
img OMIM, Score=1000, UMLKSK CUI: C0600031
HumanAIRE326autoimmune regulator
img OMIM, Score=1000, UMLKSK CUI: C0600031
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0600031Congenital absence of spleen0self