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Details
Link-It Detail - Human Phenotype - Abnormal head movements
Debug Stats
  • ### Total Build Time: 17 ms 11.122 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 198 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=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=3 ms Completed: 3 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 761 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=1 ms Completed: 1 ms rowSize= 3.010 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 5.580 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal head movements HP:0002457
Parents (1)
img Abnormality of movement HP:0100022
Children (2)
img Head titubation HP:0002599
img Jerky head movements HP:0006961
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of movement HP:0100022
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of movement HP:0100022
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of movement HP:0100022
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanSCAX3727715spinocerebellar ataxia, X-linked 3
img HP RolledUp, OMIM ID: 301790
HumanCOMA266710Cogan-type congential oculomotor apraxia
img HP RolledUp, OMIM ID: 257550
HumanGJC257165gap junction protein, gamma 2, 47kDa
img HP RolledUp, OMIM ID: 608804
HumanPLP15354proteolipid protein 1
img HP RolledUp, OMIM ID: 312080
HumanFMR12332fragile X mental retardation 1
img HP IEA, OMIM ID: 300624
img HP IEA, OMIM ID: 309550
HumanDLAT1737dihydrolipoamide S-acetyltransferase
img HP RolledUp, OMIM ID: 245348
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002457Abnormal head movements0self