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Details
Link-It Detail - Human Phenotype - Abnormality of cognition
Debug Stats
  • ### Total Build Time: 29 ms 29.084 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 199 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=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 462 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.382 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.177 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 24.553 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of cognition HP:0002302
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the central nervous system HP:0002011
Children (4)
img Dementia HP:0000726
img Cognitive decline HP:0002303
img Cognitive defects HP:0002441
img Neuropsychologic cognitive abnormalities HP:0006972
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
Genes (156)

Species:
human : 156
Page Size
Current 25
  Page 1 of 7
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
HumanAD10780912Alzheimer disease-10
img HP RolledUp, OMIM ID: 104300
img HP RolledUp, OMIM ID: 609636
HumanSCAX4727716spinocerebellar ataxia, X-linked 4
img HP RolledUp, OMIM ID: 301840
HumanSCAX3727715spinocerebellar ataxia, X-linked 3
img HP RolledUp, OMIM ID: 301790
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanPSNP2619408supranuclear palsy, progressive, 2
img HP RolledUp, OMIM ID: 609454
HumanAD9450086Alzheimer disease 9
img HP RolledUp, OMIM ID: 104300
HumanNHLRC1378884NHL repeat containing 1
img HP RolledUp, OMIM ID: 254780
HumanAD8353128Alzheimer disease 8
img HP RolledUp, OMIM ID: 104300
HumanMFSD8256471major facilitator superfamily domain containing 8
img HP RolledUp, OMIM ID: 610951
HumanC9orf72203228chromosome 9 open reading frame 72
img HP RolledUp, OMIM ID: 105550
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanLRRK2120892leucine-rich repeat kinase 2
img HP RolledUp, OMIM ID: 607060
HumanC19orf1283636chromosome 19 open reading frame 12
img HP RolledUp, OMIM ID: 614298
HumanAMN81693amnion associated transmembrane protein
img HP RolledUp, OMIM ID: 261100
HumanCOL18A180781collagen, type XVIII, alpha 1
img HP RolledUp, OMIM ID: 267750
HumanDNAJC580331DnaJ (Hsp40) homolog, subfamily C, member 5
img HP RolledUp, OMIM ID: 204300
img HP RolledUp, OMIM ID: 162350
HumanOPA380207optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
img HP RolledUp, OMIM ID: 258501
HumanPANK280025pantothenate kinase 2
img HP RolledUp, OMIM ID: 234200
img HP RolledUp, OMIM ID: 607236
HumanROGDI79641rogdi homolog (Drosophila)
img HP RolledUp, OMIM ID: 226750
HumanFA2H79152fatty acid 2-hydroxylase
img HP RolledUp, OMIM ID: 612443
img HP RolledUp, OMIM ID: 612319
HumanPINK165018PTEN induced putative kinase 1
img HP RolledUp, OMIM ID: 605909
HumanAD664851Alzheimer disease 6
img HP RolledUp, OMIM ID: 104300
HumanPARK460454Parkinson disease (autosomal dominant, Lewy body) 4
img HP RolledUp, OMIM ID: 605543
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002302Abnormality of cognition0self