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Details
Link-It Detail - Human Phenotype - Abnormality of the glial cells
Debug Stats
  • ### Total Build Time: 52 ms 30.228 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 205 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 201 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 820 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.321 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.133 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=40 ms Completed: 40 ms rowSize= 23.407 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the glial cells HP:0100705
Definition (1)
An abnormality of the `glia cell` (CL:0000125).
Parents (2)
img Abnormality of the central nervous system HP:0002011
img Morphological abnormality of the central nervous system HP:0007319
Children (7)
img Astrocytosis HP:0002446
img CNS demyelination HP:0007305
img Abnormality of the oligodendroglia HP:0100706
img Gliosis HP:0002171
img Abnormality of the astrocytes HP:0100707
img Glioma HP:0009733
img Abnormality of the microglia HP:0100708
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
img All HP:0000001img Phenotypic abnormality HP:00001186img Morphological abnormality of the central nervous system HP:0007319
Genes (128)

Species:
human : 128
Page Size
Current 25
  Page 1 of 6
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanCD24100133941CD24 molecule
img HP RolledUp, OMIM ID: 126200
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
HumanRTE1404685repressor of telomerase expression 1
img HP RolledUp, OMIM ID: 137800
HumanNDUFS7374291NADH dehydrogenase (ubiquinone) Fe-S protein 7, 20kDa (NADH-coenzyme Q reductase)
img HP RolledUp, OMIM ID: 256000
HumanGLM1338030Glioma, familial, 1
img HP RolledUp, OMIM ID: 137800
HumanSUMF1285362sulfatase modifying factor 1
img HP RolledUp, OMIM ID: 272200
HumanTSEN54283989TSEN54 tRNA splicing endonuclease subunit
img HP RolledUp, OMIM ID: 225753
img HP RolledUp, OMIM ID: 277470
HumanBRAT1221927BRCA1-associated ATM activator 1
img HP RolledUp, OMIM ID: 614498
HumanC9orf72203228chromosome 9 open reading frame 72
img HP RolledUp, OMIM ID: 105550
HumanPARK10170534Parkinson disease 10 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanARX170302aristaless related homeobox
img HP RolledUp, OMIM ID: 300215
HumanNDUFAF6137682NADH dehydrogenase (ubiquinone) complex I, assembly factor 6
img HP RolledUp, OMIM ID: 256000
HumanLRRK2120892leucine-rich repeat kinase 2
img HP RolledUp, OMIM ID: 607060
HumanNDUFAF291942NADH dehydrogenase (ubiquinone) complex I, assembly factor 2
img HP RolledUp, OMIM ID: 256000
HumanL2HGDH79944L-2-hydroxyglutarate dehydrogenase
img HP RolledUp, OMIM ID: 236792
HumanZNF33563925zinc finger protein 335
img HP RolledUp, OMIM ID: 615095
HumanKCNT157582potassium channel, subfamily T, member 1
img HP RolledUp, OMIM ID: 614959
HumanNDUFA1255967NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 12
img HP RolledUp, OMIM ID: 256000
HumanWDR1155717WD repeat domain 11
img HP RolledUp, OMIM ID: 137800
HumanFOXRED155572FAD-dependent oxidoreductase domain containing 1
img HP RolledUp, OMIM ID: 256000
HumanTREM254209triggering receptor expressed on myeloid cells 2
img HP RolledUp, OMIM ID: 221770
HumanHMSNO50989Neuropathy, hereditary motor and sensory, Okinawa type
img HP RolledUp, OMIM ID: 604484
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100705Abnormality of the glial cells0self