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Details
Link-It Detail - Human Phenotype - Abnormality of binocular vision
Debug Stats
  • ### Total Build Time: 34 ms 24.108 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 303 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=3 ms Completed: 3 ms rowSize= 442 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 753 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 2.080 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=25 ms Completed: 25 ms rowSize= 19.194 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of binocular vision HP:0011514
Definition (1)
An abnormality of binocular vision, that is of the ability to synthesize the visual inputs from both eyes to a single image with perception of depth.
Parents (1)
img Abnormality of vision HP:0000504
Children (2)
img Diplopia HP:0000651
img Abnormal stereopsis HP:0011515
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of vision HP:0000504
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of vision HP:0000504
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
HumanEA3780905Episodic ataxia, type 3
img HP RolledUp, OMIM ID: 606554
HumanNYS5780901Nystagmus 5, infantile periodic alternating
img HP RolledUp, OMIM ID: 300589
HumanPSNP2619408supranuclear palsy, progressive, 2
img HP RolledUp, OMIM ID: 609454
HumanTHM7063thymoma
img HP RolledUp, OMIM ID: 274230
HumanTGFB17040transforming growth factor, beta 1
img HP RolledUp, OMIM ID: 131300
HumanSLC2A16513solute carrier family 2 (facilitated glucose transporter), member 1
img HP RolledUp, OMIM ID: 601042
HumanRAPSN5913receptor-associated protein of the synapse
img HP RolledUp, OMIM ID: 601592
HumanPTPRC5788protein tyrosine phosphatase, receptor type, C
img HP RolledUp, OMIM ID: 126200
HumanPRNP5621prion protein
img HP RolledUp, OMIM ID: 600072
HumanSERPINI15274serpin peptidase inhibitor, clade I (neuroserpin), member 1
img HP RolledUp, OMIM ID: 604218
HumanPDCD15133programmed cell death 1
img HP RolledUp, OMIM ID: 126200
HumanNDUFV14723NADH dehydrogenase (ubiquinone) flavoprotein 1, 51kDa
img HP RolledUp, OMIM ID: 203450
HumanMS4397multiple sclerosis
img HP RolledUp, OMIM ID: 126200
HumanATXN34287ataxin 3
img HP RolledUp, OMIM ID: 109150
HumanCIITA4261class II, major histocompatibility complex, transactivator
img HP RolledUp, OMIM ID: 126200
HumanMAPT4137microtubule-associated protein tau
img HP RolledUp, OMIM ID: 601104
HumanIL7R3575interleukin 7 receptor
img HP RolledUp, OMIM ID: 126200
HumanHLA-DRB13123
img HP RolledUp, OMIM ID: 126200
HumanHLA-DQB13119
img HP RolledUp, OMIM ID: 126200
HumanGFAP2670glial fibrillary acidic protein
img HP RolledUp, OMIM ID: 203450
HumanCSE1433choreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity)
img HP RolledUp, OMIM ID: 601042
HumanCACNA1A773calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
img HP RolledUp, OMIM ID: 108500
HumanATP1A2477ATPase, Na+/K+ transporting, alpha 2 polypeptide
img HP RolledUp, OMIM ID: 602481
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011514Abnormality of binocular vision0self