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Details
Link-It Detail - Disease - CONGEN HYDROCEPHALUS
Debug Stats
  • ### Total Build Time: 104 ms 14.360 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 338 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 193 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=77 ms Completed: 77 ms rowSize= 11.252 KB
  • CONCEPT_GENES gt=10 ms Completed: 10 ms rowSize= 1.365 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.154 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
CONGEN HYDROCEPHALUS C0020256
Definition (1)
Hydrocephalus that is present at birth.
Relationships (25)

Relation Types:
diso_​to_​anat : 4
diso_​to_​diso : 21


Relationships:
associated_​with : 1
classifies : 1
is_​associated_​anatomic_​site_​of : 2
is_​primary_​anatomic_​site_​of_​disease : 1
isa : 6
location_​of : 1
mapped_​to : 13
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_ANATis_primary_anatomic_site_of_diseaseimg Brain C0006104
DISO_to_ANATis_associated_anatomic_site_ofimg Central Nervous System C0927232
DISO_to_ANATlocation_ofimg Cerebrospinal Fluid C0007806
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_DISOmapped_toimg ABSENCE OF CEREBRAL HEMISPHERES CONGEN C0020225
DISO_to_DISOmapped_toimg Aqueduct of Sylvius anomaly C0266474
DISO_to_DISOmapped_toimg Aqueduct of Sylvius obstruction, congenital C0266475
DISO_to_DISOmapped_toimg Aqueduct of Sylvius stenosis C0266476
DISO_to_DISOmapped_toimg Atresia of foramen of Luschka C0266478
DISO_to_DISOmapped_toimg Atresia of foramen of Magendie C0266477
DISO_to_DISOmapped_toimg CONGEN HYDROCEPHALUS C0020256
DISO_to_DISOmapped_toimg Chatter-box syndrome C0270719
DISO_to_DISOassociated_withimg Congenital accumulation of fluid C0333004
DISO_to_DISOisaimg Congenital hydrocephalus due to toxoplasmosis C0554616
DISO_to_DISOclassifiesimg Congenital neurologic anomalies C0497552
DISO_to_DISOisaimg Dandy-Walker Syndrome C0010964
DISO_to_DISOmapped_toimg Hydranencephaly with Proliferative Vasculopathy C0431383
DISO_to_DISOmapped_toimg Hydrocephalus associated with congenital aqueduct stenosis C0431355
DISO_to_DISOmapped_toimg Hydrocephalus associated with late onset aqueduct stenosis C0431356
DISO_to_DISOmapped_toimg Hydrocephalus with anomaly of aqueduct of Sylvius C0431358
DISO_to_DISOisaimg Hydromyelocele with hydrocephalus C0431316
DISO_to_DISOisaimg Myelocele with hydrocephalus C0344474
DISO_to_DISOisaimg Rachischisis with hydrocephalus C0431315
DISO_to_DISOisaimg Spina bifida with hydrocephalus of late onset C0431314
DISO_to_DISOmapped_toimg X-linked hydrocephalus syndrome C0265216
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanL1CAM3897L1 cell adhesion molecule
img OMIM, Score=882, UMLKSK CUI: C0020256
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020256CONGEN HYDROCEPHALUS0self