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Details
Link-It Detail - Disease - Glycogen Storage Disease Type VI
Debug Stats
  • ### Total Build Time: 36 ms 10.288 KB
  • CONCEPT_NAME gt=15 ms Completed: 15 ms rowSize= 362 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 301 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=3 ms Completed: 3 ms rowSize= 560 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.847 KB
  • CONCEPT_RELATIONSHIPS gt=16 ms Completed: 16 ms rowSize= 4.818 KB
  • CONCEPT_GENES gt=2 ms Completed: 2 ms rowSize= 45 bytes
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Glycogen Storage Disease Type VI C0017925
Definition (1)
A hepatic GLYCOGEN STORAGE DISEASE in which there is an apparent deficiency of hepatic phosphorylase (GLYCOGEN PHOSPHORYLASE, LIVER FORM) activity.
Semantic Types (1)
Disease or Syndrome (T047)
Parents (1)
img Glycogen Storage Disease C0017919
Ancestral Roots
RootRoot Plus OneDepthParent
img Congenital, Hereditary, and Neonatal Diseases and Abnormalities C0027612img Genetic Diseases, Inborn C09501236img Glycogen Storage Disease C0017919
img Nutritional and Metabolic Diseases C0028715img Metabolic Diseases C00255176img Glycogen Storage Disease C0017919
Relationships (9)

Relation Types:
diso_​to_​chem : 3
diso_​to_​diso : 4
diso_​to_​phen : 1
diso_​to_​phys : 1


Relationships:
none : 5
associated_​with : 3
use : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_CHEM1img Glycogen Phosphorylase, Liver Form C0969684
DISO_to_DISO1img Complication Aspects C1171258
DISO_to_DISO1img Focal Nodular Hyperplasia C0333980
DISO_to_PHEN1img genetic aspects C0017399
DISO_to_PHYS1img Mutation C0026882
DISO_to_CHEMassociated_withimg Glycogen C0017911
DISO_to_CHEMassociated_withimg Glycogen Phosphorylase, Muscle Form C0917783
DISO_to_DISOassociated_withimg 270 CONGENITAL DEFICIENCIES C0333006
DISO_to_DISOuseimg Glycogen Storage Disease Type VI C0017925
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0017925Glycogen Storage Disease Type VI0self