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Details
Link-It Detail - Human Phenotype - Abnormality of somatosensory evoked potentials
Debug Stats
  • ### Total Build Time: 31 ms 30.176 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 221 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
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 795 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.810 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 3.041 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 23.148 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.040 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of somatosensory evoked potentials HP:0007377
Parents (2)
img Neurophysiological abnormality HP:0001311
img Abnormality of the sensory nervous system HP:0001333
Children (5)
img Prolonged somatosensory evoked potentials HP:0007104
img Abnormality of central somatosensory evoked potentials HP:0100291
img Abnormality of peripheral somatosensory evoked potentials HP:0100290
img Enhancement of the C-reflex HP:0001340
img Giant somatosensory evoked potentials HP:0001312
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Neurophysiological abnormality HP:0001311
img All HP:0000001img Phenotypic abnormality HP:00001185img Neurophysiological abnormality HP:0001311
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the sensory nervous system HP:0001333
Genes (51)

Species:
human : 51
Page Size
Current 25
  Page 1 of 3
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanFAME4101409188Epilepsy, familial adult myoclonic, 4
img HP RolledUp, OMIM ID: 615127
HumanFAME3100529229Epilepsy, familial adult myoclonic, 3
img HP RolledUp, OMIM ID: 613608
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanISPD729920isoprenoid synthase domain containing
img HP RolledUp, OMIM ID: 614643
HumanEPRPDC574044Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp
img HP RolledUp, OMIM ID: 608105
HumanFCMTE2554188familial cortical myoclonic tremor with epilepsy 2
img HP RolledUp, OMIM ID: 607876
HumanKIF7374654kinesin family member 7
img HP RolledUp, OMIM ID: 200990
HumanH19283120H19, imprinted maternally expressed transcript (non-protein coding)
img HP RolledUp, OMIM ID: 130650
HumanHYLS1219844hydrolethalus syndrome 1
img HP RolledUp, OMIM ID: 236680
HumanASXL1171023additional sex combs like 1 (Drosophila)
img HP RolledUp, OMIM ID: 605039
HumanEVC2132884Ellis van Creveld syndrome 2
img HP RolledUp, OMIM ID: 225500
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 607361
HumanCEP29080184centrosomal protein 290kDa
img HP RolledUp, OMIM ID: 611134
HumanFKRP79147fukutin related protein
img HP RolledUp, OMIM ID: 236670
img HP RolledUp, OMIM ID: 613153
HumanFTO79068fat mass and obesity associated
img HP RolledUp, OMIM ID: 612938
HumanTMEM23765062transmembrane protein 237
img HP RolledUp, OMIM ID: 614424
HumanNSD164324nuclear receptor binding SET domain protein 1
img HP RolledUp, OMIM ID: 130650
HumanFLVCR255640feline leukemia virus subgroup C cellular receptor family, member 2
img HP RolledUp, OMIM ID: 225790
HumanCHD755636chromodomain helicase DNA binding protein 7
img HP RolledUp, OMIM ID: 214800
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 249000
HumanTMEM13851524transmembrane protein 138
img HP RolledUp, OMIM ID: 614465
HumanFCMTE150968familial cortical myoclonic tremor with epilepsy 1
img HP RolledUp, OMIM ID: 601068
HumanPOMT229954protein-O-mannosyltransferase 2
img HP RolledUp, OMIM ID: 236670
HumanNPHP327031nephronophthisis 3 (adolescent)
img HP RolledUp, OMIM ID: 208540
img HP RolledUp, OMIM ID: 267010
HumanATP6V0A223545ATPase, H+ transporting, lysosomal V0 subunit a2
img HP RolledUp, OMIM ID: 219200
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0007377Abnormality of somatosensory evoked potentials0self