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Details
Link-It Detail - Human Phenotype - Abnormality of eye movement
Debug Stats
  • ### Total Build Time: 51 ms 39.147 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
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  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 8.855 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 4.858 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=49 ms Completed: 49 ms rowSize= 23.319 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of eye movement HP:0000496
Parents (2)
img Abnormality of movement HP:0100022
img Abnormality of the eye HP:0000478
Children (27)
img Globe retraction and deviation on adduction HP:0001109
img Severe limitations of eye movements HP:0007959
img Impaired ocular abduction HP:0000634
img Limited extraocular movements HP:0007941
img Chaotic rapid conjugate ocular movements HP:0007295
img Abnormality of the extraocular muscles HP:0008049
img Opsoclonus HP:0010543
img Oculomotor abnormalities HP:0006860
img Abnormal rapid eye movement (REM) sleep HP:0002494
img Disconjugate eye movements HP:0000549
img Defective or absent horizontal voluntary eye movements HP:0007764
img Abnormality of saccadic eye movements HP:0000570
img Abnormality of ocular abduction HP:0011347
img Abnormal, jerky eye movements HP:0000628
img Compensatory chin elevation HP:0001477
img Impaired convergence HP:0000619
img Oculomotor apraxia HP:0000657
img Ophthalmoparesis HP:0000597
img Strabismus HP:0000486
img Abnormality of ocular smooth pursuit HP:0000617
img Globe retraction and deviation on abduction HP:0000497
img Impaired ocular adduction HP:0000542
img Uncontrolled eye movements HP:0007738
img Nystagmus HP:0000639
img Prominent eyes HP:0000536
img Paroxysmal involuntary eye movements HP:0007704
img Duane anomaly HP:0009921
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of movement HP:0100022
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of movement HP:0100022
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of movement HP:0100022
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the eye HP:0000478
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the eye HP:0000478
Genes (769)

Species:
human : 769
Page Size
Current 25
  Page 1 of 31
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanNYS7101055624Nystagmus 7, congenital
img HP RolledUp, OMIM ID: 614826
HumanDELXQ21100887743Choroideremia, deafness, and mental retardation
img HP RolledUp, OMIM ID: 303110
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanSCAR12100820764Spinocerebellar ataxia, autosomal recessive 12
img HP RolledUp, OMIM ID: 614322
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanSCA34100750330spinocerebellar ataxia 34
img HP RolledUp, OMIM ID: 133190
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanLCR-OPSIN100534624
img HP RolledUp, OMIM ID: 303700
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL4Q21100528026Chromosome 4q21 deletion syndrome
img HP RolledUp, OMIM ID: 613509
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanOCLN100506658occludin
img HP RolledUp, OMIM ID: 251290
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanSPAX3100379201Ataxia, spastic, 3, autosomal recessive
img HP RolledUp, OMIM ID: 611390
HumanSCA30100359393spinocerebellar ataxia 30
img HP RolledUp, OMIM ID: 613371
HumanSPG45100322879spastic paraplegia 45 (autosomal recessive)
img HP RolledUp, OMIM ID: 613162
HumanSCA31100312950spinocerebellar ataxia 31
img HP RolledUp, OMIM ID: 117210
HumanLKMCD100302058Leukoencephalopathy with metaphyseal chondrodysplasia
img HP RolledUp, OMIM ID: 300660
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP RolledUp, OMIM ID: 612626
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000496Abnormality of eye movement0self