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Details
Link-It Detail - Disease - Abnormal VEP ICD9CM:794.13
Debug Stats
  • ### Total Build Time: 80 ms 12.555 KB
  • CONCEPT_NAME gt=7 ms Completed: 7 ms rowSize= 350 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=1 ms Completed: 1 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=44 ms Completed: 44 ms rowSize= 5.332 KB
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 5.650 KB
  • CONCEPT_XREFS gt=12 ms Completed: 12 ms rowSize= 1.160 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Abnormal VEP ICD9CM:794.13 C0522214
Relationships (11)

Relation Types:
diso_​to_​diso : 6
diso_​to_​phen : 5


Relationships:
classifies : 2
mapped_​to : 8
replaces : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOreplacesimg Abnormal VEP ICD9CM:794.13 C0522214
DISO_to_DISOmapped_toimg Interocular latency asymmetry C0456443
DISO_to_DISOclassifiesimg Other and unspecified disorders of the nervous system C0154725
DISO_to_DISOclassifiesimg Other nervous system symptoms and disorders C0810273
DISO_to_DISOmapped_toimg Symmetrical visually evoked potentials C0456442
DISO_to_DISOmapped_toimg Visual evoked potential finding C0456345
DISO_to_PHENmapped_toimg Interhemisphere crossed amplitude asymmetry C0456448
DISO_to_PHENmapped_toimg Interhemisphere crossed latency asymmetry C0456446
DISO_to_PHENmapped_toimg Interhemisphere uncrossed amplitude asymmetry C0456449
DISO_to_PHENmapped_toimg Interhemisphere uncrossed latency asymmetry C0456447
DISO_to_PHENmapped_toimg Interhemisphere uncrossed waveform asymmetry C0456451
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanSLC25A2279751solute carrier family 25 (mitochondrial carrier: glutamate), member 22
img OMIM, Score=1000, UMLKSK CUI: C0522214
HumanMFN29927mitofusin 2
img OMIM, Score=1000, UMLKSK CUI: C0522214
HumanPLA2G68398phospholipase A2, group VI (cytosolic, calcium-independent)
img OMIM, Score=1000, UMLKSK CUI: C0522214
HumanAAAS8086achalasia, adrenocortical insufficiency, alacrimia
img OMIM, Score=1000, UMLKSK CUI: C0522214
HumanPOLG5428polymerase (DNA directed), gamma
img OMIM, Score=1000, UMLKSK CUI: C0522214
HumanGALC2581galactosylceramidase
img OMIM, Score=900, UMLKSK CUI: C0522214
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0522214Abnormal VEP ICD9CM:794.130self