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Details
Link-It Detail - Disease - Leukomalacia, Periventricular
Debug Stats
  • ### Total Build Time: 103 ms 29.523 KB
  • CONCEPT_NAME gt=13 ms Completed: 13 ms rowSize= 419 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 631 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=2 ms Completed: 2 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= 1.407 KB
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=18 ms Completed: 18 ms rowSize= 5.416 KB
  • CONCEPT_RELATIONSHIPS gt=34 ms Completed: 34 ms rowSize= 12.627 KB
  • CONCEPT_GENES gt=17 ms Completed: 17 ms rowSize= 7.666 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.163 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Leukomalacia, Periventricular C0023529
Encephalomalacia, Periventricular
Definition (1)
Degeneration of white matter adjacent to the CEREBRAL VENTRICLES following cerebral hypoxia or BRAIN ISCHEMIA in neonates. The condition primarily affects white matter in the perfusion zone between superficial and deep branches of the MIDDLE CEREBRAL ARTERY. Clinical manifestations include VISION DISORDERS; CEREBRAL PALSY; PARAPLEGIA; SEIZURES; and cognitive disorders. (From Adams et al., Principles of Neurology, 6th ed, p1021; Joynt, Clinical Neurology, 1997, Ch4, pp30-1)
Semantic Types (1)
Disease or Syndrome (T047)
Parents (3)
img Cerebrovascular Disorders C0007820
img Encephalomalacia C0014068
img Infant, Premature, Diseases C0021295
Ancestral Roots
RootRoot Plus OneDepthParent
img Cardiovascular Diseases C0007222img Vascular Diseases C00423734img Cerebrovascular Disorders C0007820
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Cerebrovascular Disorders C0007820
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Encephalomalacia C0014068
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Infant, Newborn, Diseases C00212904img Infant, Premature, Diseases C0021295
Relationships (36)

Relation Types:
diso_​to_​anat : 12
diso_​to_​diso : 23
diso_​to_​phen : 1


Relationships:
none : 29
classifies : 2
expanded_​form_​of : 1
is_​associated_​anatomic_​site_​of : 2
isa : 1
mapped_​to : 1
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISO39img Complication Aspects C1171258
DISO_to_ANAT35img Brain C0006104
DISO_to_DISO31img Cerebral Hemorrhage C2937358
DISO_to_DISO31img INFANT PREMATURE DIS C0021295
DISO_to_DISO24img Cerebral Palsy C0007789
DISO_to_DISO24img INFANT PREMATURE DIS C0021295
DISO_to_ANAT23img Brain C0006104
DISO_to_DISO23img Complication Aspects C1171258
DISO_to_DISO21img Cerebral Palsy C0007789
DISO_to_ANAT15img Myelinated nerve fiber C0027750
DISO_to_DISO14img Cerebral Hemorrhage C2937358
DISO_to_DISO11img Brain Hypoxia Ischemia C0752308
DISO_to_DISO11img INFANT VLBW C0282667
DISO_to_ANAT10img In Blood C0005768
DISO_to_ANAT9img Cerebral Ventricles C0007799
DISO_to_ANAT9img In Blood C0005768
DISO_to_DISO9img Brain Hypoxia Ischemia C0752308
DISO_to_DISO9img Developmental Disabilities C0008073
DISO_to_PHEN9img genetic aspects C0017399
DISO_to_ANAT8img Cerebral Cortex C0007776
DISO_to_ANAT8img Neurons C0027882
DISO_to_ANAT7img Cerebral Ventricles C0007799
DISO_to_ANAT7img Oligodendrocyte C0028944
DISO_to_DISO7img BRAIN SYNDROME CHRONIC C0006109
DISO_to_DISO7img Developmental Disabilities C0008073
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanTREX111277three prime repair exonuclease 1
img OMIM, Score=1000, UMLKSK CUI: C0023529
HumanSLC1A26506solute carrier family 1 (glial high affinity glutamate transporter), member 2
img GENERIF, Score=1000, Pubmed Id: 17311320, UMLKSK CUI: C0023529
HumanPC5091pyruvate carboxylase
img OMIM, Score=1000, UMLKSK CUI: C0023529
HumanMYT14661myelin transcription factor 1
img GENERIF, Score=1000, Pubmed Id: 12524179, UMLKSK CUI: C0023529
HumanIL183606interleukin 18 (interferon-gamma-inducing factor)
img GENERIF, Score=1000, Pubmed Id: 11895335, UMLKSK CUI: C0023529
HumanIL23558interleukin 2
img GENERIF, Score=1000, Pubmed Id: 11940709, UMLKSK CUI: C0023529
HumanEPO2056erythropoietin
img GENERIF, Score=1000, Pubmed Id: 18160550, UMLKSK CUI: C0023529
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0023529Leukomalacia, Periventricular0self