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Details
Link-It Detail - Disease - Reye Syndrome
Debug Stats
  • ### Total Build Time: 21 ms 17.256 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 385 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 534 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= 188 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 990 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 4.081 KB
  • CONCEPT_RELATIONSHIPS gt=12 ms Completed: 12 ms rowSize= 9.900 KB
  • CONCEPT_GENES gt=0 Completed: 0 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (2)
Reye Syndrome C0035400
FATTY LIVER WITH ENCEPHALOPATHY
Definition (1)
rare, acute, sometimes fatal disease of childhood, most often occurring as a sequel of varicella or a viral upper respiratory infection of childhood; marked by recurrent vomiting and elevated serum transaminase levels with distinctive changes in the liver and other viscera; an encephalopathic phase with acute brain swelling disturbances of consciousness and seizures may follow.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (2)
img Fatty Liver C0015695
img Brain Diseases, Metabolic C0006112
Ancestral Roots
RootRoot Plus OneDepthParent
img Digestive System Diseases C0012242img Liver Diseases C00238954img Fatty Liver C0015695
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255174img Brain Diseases, Metabolic C0006112
img Nervous System Diseases C0027765img Central Nervous System Diseases C00076825img Brain Diseases, Metabolic C0006112
Relationships (22)

Relation Types:
diso_​to_​chem : 13
diso_​to_​diso : 9


Relationships:
none : 4
associated_​with : 2
classifies : 2
mapped_​to : 3
may_​treat : 10
related_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM18img 2-(Acetyloxy)benzoic Acid C0004057
DISO_to_DISO15img chemically induced C0007994
DISO_to_CHEM12img 603-604 NON-STEROIDAL ANTI-INFLAMMATORY AGENTS C0003211
DISO_to_DISO8img chemically induced C0007994
DISO_to_CHEMmay_treatimg 1-Piperazineethanol, 4-(3-(2-chloro-10H-phenothiazin-10-yl)propyl)- C0031184
DISO_to_CHEMassociated_withimg Acyl CoA Dehydrogenases C0085744
DISO_to_CHEMmay_treatimg METFORMIN HYDROCHLORIDE 500 MG / PERPHENAZINE 8 MG ORAL TABLET [PERPHENAZINE] C0689944
DISO_to_CHEMmay_treatimg PERPHENAZINE 16 MG ORAL SOLUTION C0979403
DISO_to_CHEMmay_treatimg PERPHENAZINE 16 MG ORAL TABLET C0689939
DISO_to_CHEMmay_treatimg PERPHENAZINE 2 MG ORAL TABLET C0689941
DISO_to_CHEMmay_treatimg PERPHENAZINE 2MG TAB,SA C0982827
DISO_to_CHEMmay_treatimg PERPHENAZINE 4 MG ORAL TABLET C0689942
DISO_to_CHEMmay_treatimg PERPHENAZINE 4MG TAB,SA C0979404
DISO_to_CHEMmay_treatimg PERPHENAZINE 5 MG/ML Injection (systemic) solution C0774200
DISO_to_CHEMmay_treatimg PERPHENAZINE 8 mg ORAL TABLET, SUSTAINED ACTION C0979406
DISO_to_DISOassociated_withimg 270 CONGENITAL DEFICIENCIES C0333006
DISO_to_DISOmapped_toimg Blepharospasm C0005747
DISO_to_DISOmapped_toimg FATTY LIVER WITH ENCEPHALOPATHY C0035400
DISO_to_DISOrelated_toimg Liver Diseases C0023895
DISO_to_DISOmapped_toimg Medium-chain acyl-coenzyme A dehydrogenase deficiency C0220710
DISO_to_DISOclassifiesimg Other and unspecified hereditary and degenerative nervous conditions C0810267
DISO_to_DISOclassifiesimg Other hereditary and degenerative nervous system conditions C0809991
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0035400Reye Syndrome0self