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Details
Link-It Detail - Human Phenotype - Abnormality of the globus pallidus
Debug Stats
  • ### Total Build Time: 17 ms 9.528 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 206 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=2 ms Completed: 2 ms rowSize= 453 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.104 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 3.971 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 2.433 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the globus pallidus HP:0002453
Definition (1)
An abnormality of the `globus pallidus` (FMA:61835).
Parents (1)
img Abnormality of the basal ganglia HP:0002134
Children (3)
img Eye of the tiger anomaly of globus pallidus HP:0002454
img Severe involvement of globus pallidus HP:0007040
img Pallidal degeneration HP:0007132
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the basal ganglia HP:0002134
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the basal ganglia HP:0002134
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the basal ganglia HP:0002134
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the basal ganglia HP:0002134
Genes (2)

Species:
human : 2
SpeciesGeneGeneIdGene NameEvidence
HumanPANK280025pantothenate kinase 2
img HP RolledUp, OMIM ID: 607236
img HP RolledUp, OMIM ID: 234200
HumanMUT4594methylmalonyl CoA mutase
img HP IEA, OMIM ID: 251000
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002453Abnormality of the globus pallidus0self