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GATACA
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Details
Link-It Detail - Human Phenotype - Abnormality of the hamate bone
Debug Stats
  • ### Total Build Time: 17 ms 12.002 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 205 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=4 ms Completed: 4 ms rowSize= 452 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 1.060 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 3.968 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 5.164 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the hamate bone HP:0004259
Parents (1)
img Abnormality of the carpal bones HP:0001191
Children (3)
img Large hamate bone HP:0004260
img Wide hamate bone HP:0004261
img Capitate-hamate fusion HP:0001241
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the carpal bones HP:0001191
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the carpal bones HP:0001191
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the carpal bones HP:0001191
img All HP:0000001img Phenotypic abnormality HP:000011811img Abnormality of the carpal bones HP:0001191
Genes (6)

Species:
human : 6
SpeciesGeneGeneIdGene NameEvidence
HumanACRPV414058Acropectorovertebral dysplasia (F syndrome)
img HP RolledUp, OMIM ID: 102510
HumanEVC2132884Ellis van Creveld syndrome 2
img HP RolledUp, OMIM ID: 225500
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 311300
HumanFGFR32261fibroblast growth factor receptor 3
img HP RolledUp, OMIM ID: 602849
HumanEVC2121Ellis van Creveld syndrome
img HP RolledUp, OMIM ID: 225500
HumanATP7A538ATPase, Cu++ transporting, alpha polypeptide
img HP RolledUp, OMIM ID: 304150
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0004259Abnormality of the hamate bone0self