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Details
Link-It Detail - Human Phenotype - Abnormality of nail color
Debug Stats
  • ### Total Build Time: 18 ms 13.108 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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= 444 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.040 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 3.010 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=8 ms Completed: 8 ms rowSize= 7.066 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of nail color HP:0100643
Definition (1)
An anomaly of the color of the `nail` (FMA:54326).
Parents (1)
img Abnormality of the nail HP:0001597
Children (3)
img Leukonychia HP:0001820
img Melanonychia HP:0100644
img Yellow nails HP:0011367
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nail HP:0001597
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the nail HP:0001597
Genes (8)

Species:
human : 8
SpeciesGeneGeneIdGene NameEvidence
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP TAS, OMIM ID: 611775
HumanABCA1226154ATP-binding cassette, sub-family A (ABC1), member 12
img HP RolledUp, OMIM ID: 601277
HumanGJB610804gap junction protein, beta 6, 30kDa
img HP TAS, OMIM ID: 129500
HumanTRPS17227trichorhinophalangeal syndrome I
img HP RolledUp, OMIM ID: 190350
HumanPLCD15333phospholipase C, delta 1
img HP RolledUp, OMIM ID: 151600
HumanKIF113832kinesin family member 11
img HP TAS, OMIM ID: 152950
HumanGJB22706gap junction protein, beta 2, 26kDa
img HP TAS, OMIM ID: 149200
HumanFOXC22303forkhead box C2 (MFH-1, mesenchyme forkhead 1)
img HP RolledUp, OMIM ID: 153200
img HP TAS, OMIM ID: 153300
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0100643Abnormality of nail color0self