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Details
Link-It Detail - Human Phenotype - Abnormality of the caudate nucleus
Debug Stats
  • ### Total Build Time: 21 ms 13.212 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=0 Completed: 0 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= 778 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 473 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=8 ms Completed: 8 ms rowSize= 6.740 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 3.672 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the caudate nucleus HP:0002339
Definition (1)
An abnormality of the `caudate nucleus` (FMA:61833).
Parents (2)
img Abnormality of the cerebrum HP:0002060
img Abnormality of the striatum HP:0010994
Children (1)
img Atrophy/Degeneration involving the caudate nucleus HP:0007374
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the cerebrum HP:0002060
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the striatum HP:0010994
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the striatum HP:0010994
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the striatum HP:0010994
img All HP:0000001img Phenotypic abnormality HP:000011811img Abnormality of the striatum HP:0010994
Genes (4)

Species:
human : 4
SpeciesGeneGeneIdGene NameEvidence
HumanTREM254209triggering receptor expressed on myeloid cells 2
img HP RolledUp, OMIM ID: 221770
HumanHLN253369Huntington-like neurodegenerative disorder 2
img HP RolledUp, OMIM ID: 604802
HumanVPS13A23230vacuolar protein sorting 13 homolog A (S. cerevisiae)
img HP RolledUp, OMIM ID: 200150
HumanTYROBP7305TYRO protein tyrosine kinase binding protein
img HP RolledUp, OMIM ID: 221770
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002339Abnormality of the caudate nucleus0self