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Details
Link-It Detail - Human Phenotype - Abnormality of balance
Debug Stats
  • ### Total Build Time: 21 ms 25.509 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 197 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=2 ms Completed: 2 ms rowSize= 462 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 437 bytes
  • 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=13 ms Completed: 13 ms rowSize= 21.937 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.017 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of balance HP:0100683
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the central nervous system HP:0002011
Children (1)
img Gait imbalance HP:0002141
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the central nervous system HP:0002011
Genes (26)

Species:
human : 26
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanBPPV619536vestibulopathy, familial
img HP RolledUp, OMIM ID: 193007
HumanPSNP2619408supranuclear palsy, progressive, 2
img HP RolledUp, OMIM ID: 609454
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanBBS5129880Bardet-Biedl syndrome 5
img HP RolledUp, OMIM ID: 209900
HumanTTC8123016tetratricopeptide repeat domain 8
img HP RolledUp, OMIM ID: 209900
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanTMEM6791147transmembrane protein 67
img HP RolledUp, OMIM ID: 209900
HumanARL684100ADP-ribosylation factor-like 6
img HP RolledUp, OMIM ID: 209900
HumanCEP29080184centrosomal protein 290kDa
img HP RolledUp, OMIM ID: 209900
HumanBBS1079738Bardet-Biedl syndrome 10
img HP RolledUp, OMIM ID: 209900
HumanCCDC28B79140coiled-coil domain containing 28B
img HP RolledUp, OMIM ID: 209900
HumanBBS755212Bardet-Biedl syndrome 7
img HP RolledUp, OMIM ID: 209900
HumanMKS154903Meckel syndrome, type 1
img HP RolledUp, OMIM ID: 209900
HumanMLXIPL51085MLX interacting protein-like
img HP RolledUp, OMIM ID: 194050
HumanWDPCP51057WD repeat containing planar cell polarity effector
img HP RolledUp, OMIM ID: 209900
HumanBBS927241Bardet-Biedl syndrome 9
img HP RolledUp, OMIM ID: 209900
HumanTRIM3222954tripartite motif containing 32
img HP RolledUp, OMIM ID: 209900
HumanSDCCAG810806serologically defined colon cancer antigen 8
img HP RolledUp, OMIM ID: 209900
HumanGTF2IRD19569GTF2I repeat domain containing 1
img HP RolledUp, OMIM ID: 194050
HumanMKKS8195McKusick-Kaufman syndrome
img HP RolledUp, OMIM ID: 209900
HumanMAPT4137microtubule-associated protein tau
img HP RolledUp, OMIM ID: 601104
HumanGTF2I2969general transcription factor IIi
img HP RolledUp, OMIM ID: 194050
HumanELN2006elastin
img HP RolledUp, OMIM ID: 194050
HumanBBS4585Bardet-Biedl syndrome 4
img HP RolledUp, OMIM ID: 209900
HumanBBS2583Bardet-Biedl syndrome 2
img HP RolledUp, OMIM ID: 209900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100683Abnormality of balance0self