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Details
Link-It Detail - Disease - Hydranencephaly
Debug Stats
  • ### Total Build Time: 96 ms 11.015 KB
  • CONCEPT_NAME gt=9 ms Completed: 9 ms rowSize= 396 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 402 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=24 ms Completed: 24 ms rowSize= 191 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 564 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.854 KB
  • CONCEPT_RELATIONSHIPS gt=47 ms Completed: 47 ms rowSize= 5.416 KB
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.149 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Hydranencephaly C0020225
ABSENCE OF CEREBRAL HEMISPHERES CONGEN
Definition (1)
A rare congenital brain disorder in which the cerebral hemispheres are absent and replaced by sacs that contain cerebrospinal fluid. Signs and symptoms include irritability, increased muscle tone, seizures, and hydrocephalus. The prognosis is poor.
Semantic Types (1)
Congenital Abnormality (T019)
Parents (1)
img Nervous System Malformations C0497552
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Congenital Abnormalities C00007684img Nervous System Malformations C0497552
img Nervous System Diseases C0027765img Nervous System Malformations C04975523img Nervous System Malformations C0497552
Relationships (10)

Relation Types:
diso_​to_​anat : 2
diso_​to_​diso : 7
diso_​to_​phen : 1


Relationships:
none : 5
entry_​version_​of : 1
is_​associated_​anatomic_​site_​of : 2
isa : 1
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO5img BOVINE DIS C0007453
DISO_to_DISO5img COMPL PREGN INFECT C0032965
DISO_to_PHEN5img genetic aspects C0017399
DISO_to_DISO4img Blue Tongue C0005866
DISO_to_DISO4img DISORDER FETAL C0015929
DISO_to_ANATis_associated_anatomic_site_ofimg Central Nervous System C0927232
DISO_to_ANATis_associated_anatomic_site_ofimg Nervous System C0027763
DISO_to_DISOentry_version_ofimg ABSENCE OF CEREBRAL HEMISPHERES CONGEN C0020225
DISO_to_DISOisaimg Hydranencephaly with Proliferative Vasculopathy C0431383
DISO_to_DISOmapped_toimg MICROHYDRANENCEPHALY C1857977
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0020225Hydranencephaly0self