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Details
Link-It Detail - Disease - ACAD9 DEFICIENCY
Debug Stats
  • ### Total Build Time: 39 ms 15.154 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 330 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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= 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=29 ms Completed: 29 ms rowSize= 12.129 KB
  • CONCEPT_GENES gt=4 ms Completed: 4 ms rowSize= 1.482 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.150 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
ACAD9 DEFICIENCY C1970173
Relationships (29)

Relation Types:
diso_​to_​diso : 29


Relationships:
alias_​of : 1
manifestation_​of : 28
Page Size
Current 25
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Current 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOalias_ofimg ACAD9 DEFICIENCY C1970173
DISO_to_DISOmanifestation_ofimg ACIDOSIS LACTIC C0001125
DISO_to_DISOmanifestation_ofimg Cardiomyopathy, Dilated C0007193
DISO_to_DISOmanifestation_ofimg Cardiomyopathy, Hypertrophic C0007194
DISO_to_DISOmanifestation_ofimg Caused by mutation in the acyl-CoA dehydrogenase-9 gene (ACAD9, 611103.0001) C2674390
DISO_to_DISOmanifestation_ofimg Cerebellar stroke C2674383
DISO_to_DISOmanifestation_ofimg Cerebral Edema C0006114
DISO_to_DISOmanifestation_ofimg Clinical presentation varies C2674391
DISO_to_DISOmanifestation_ofimg Congestive heart failure C0018802
DISO_to_DISOmanifestation_ofimg Decreased mitochondrial complex I activity C2677650
DISO_to_DISOmanifestation_ofimg ELEVATED LACTATE DEHYDROGENASE C0151754
DISO_to_DISOmanifestation_ofimg EXERCISE INTOLERANCE C0241885
DISO_to_DISOmanifestation_ofimg Elevated liver transaminases C2674385
DISO_to_DISOmanifestation_ofimg Elevated long-chain acylcarnitine species (in some patients) C3149982
DISO_to_DISOmanifestation_ofimg Elevated plasma ammonia C2674384
DISO_to_DISOmanifestation_ofimg Elevated prothrombin time C2674387
DISO_to_DISOmanifestation_ofimg Elevated serum lactate C2674386
DISO_to_DISOmanifestation_ofimg Encephalopathies C0085584
DISO_to_DISOmanifestation_ofimg Favorable response to treatment with riboflavin C3149984
DISO_to_DISOmanifestation_ofimg Hypoglycemia C0020615
DISO_to_DISOmanifestation_ofimg Hypoketotic dicarboxylic aciduria (in some patients) C3149981
DISO_to_DISOmanifestation_ofimg Liver Failure C0085605
DISO_to_DISOmanifestation_ofimg Microvesicular steatosis C1850415
DISO_to_DISOmanifestation_ofimg Muscle Hypotonia C0026827
DISO_to_DISOmanifestation_ofimg Muscle Weakness C0151786
Genes (1)

Species:
human : 1
SpeciesGeneGeneIdGene NameEvidence
HumanACAD928976acyl-CoA dehydrogenase family, member 9
img GENERIF, Score=1000, Pubmed Id: 17564966, UMLKSK CUI: C1970173
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C1970173ACAD9 DEFICIENCY0self