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Details
Link-It Detail - Disease - Hyperreflexia
Debug Stats
  • ### Total Build Time: 76 ms 28.048 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 324 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
  • CONCEPT_NAMESPACE gt=NONE 1 ms Completed: 1 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=20 ms Completed: 20 ms rowSize= 1.983 KB
  • CONCEPT_GENES gt=36 ms Completed: 36 ms rowSize= 24.530 KB
  • CONCEPT_XREFS gt=16 ms Completed: 16 ms rowSize= 1.147 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Disease (1)
Hyperreflexia C0151889
Relationships (3)

Relation Types:
diso_​to_​diso : 3


Relationships:
isa : 2
mapped_​to : 1
Relation TypeCo-Occuring
Concept Count
RelationshipConcept
DISO_to_DISOmapped_toimg Hyperreflexia C0151889
DISO_to_DISOisaimg O/E - reflexes exaggerated C0437372
DISO_to_DISOisaimg O/E -suprapat.jerk exaggerated C0437387
Genes (109)

Species:
human : 109
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSLC6A19340024solute carrier family 6 (neutral amino acid transporter), member 19
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanARX170302aristaless related homeobox
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanTTBK2146057tau tubulin kinase 2
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanNIPA1123606non imprinted in Prader-Willi/Angelman syndrome 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanGRDX117189Graves disease, susceptibility to, X-linked
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanFAM126A84668family with sequence similarity 126, member A
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanSPG1180208spastic paraplegia 11 (autosomal recessive)
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanMCPH179648microcephalin 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanC20orf779133
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanPINK165018PTEN induced putative kinase 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanNSD164324nuclear receptor binding SET domain protein 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanIFIH164135interferon induced with helicase C domain 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanALS257679amyotrophic lateral sclerosis 2 (juvenile)
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanJPH357338junctophilin 3
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanMCOLN157192mucolipin 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanMCCC156922methylcrotonoyl-CoA carboxylase 1 (alpha)
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanC10orf256652chromosome 10 open reading frame 2
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanATL151062atlastin GTPase 1
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanGRD250976Graves disease, susceptibility to, 2
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanNDUFAF429078NADH dehydrogenase (ubiquinone) complex I, assembly factor 4
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanBSCL226580Berardinelli-Seip congenital lipodystrophy 2 (seipin)
img OMIM, Score=1000, UMLKSK CUI: C0151889
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanSACS26278spastic ataxia of Charlevoix-Saguenay (sacsin)
img OMIM, Score=1000, UMLKSK CUI: C0151889
HumanCHMP2B25978charged multivesicular body protein 2B
img OMIM, Score=1000, UMLKSK CUI: C0151889
XRefs (1)

XRef Types:
cui : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
CUIimg C0151889Hyperreflexia0self