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Details
Link-It Detail - Human Phenotype - Abnormality of dental color
Debug Stats
  • ### Total Build Time: 32 ms 15.505 KB
  • CONCEPT_NAME gt=14 ms Completed: 14 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 192 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= 452 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.068 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 1.168 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=9 ms Completed: 9 ms rowSize= 11.276 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of dental color HP:0011073
Definition (1)
A developmental defect of tooth color.
Parents (1)
img Abnormality of dental structure HP:0011061
Children (3)
img Yellow-brown discoloration of the teeth HP:0006286
img Grayish enamel HP:0000683
img Green teeth HP:0011075
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of dental structure HP:0011061
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanAA1100034700Alopecia areata 1
img HP TAS, OMIM ID: 104000
HumanROGDI79641rogdi homolog (Drosophila)
img HP TAS, OMIM ID: 226750
HumanCNNM426504cyclin M4
img HP TAS, OMIM ID: 217080
HumanENAM10117enamelin
img HP RolledUp, OMIM ID: 204650
HumanUROS7390uroporphyrinogen III synthase
img HP TAS, OMIM ID: 263700
HumanPIK3CA5290phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha
img HP TAS, OMIM ID: 162900
HumanNTRK14914neurotrophic tyrosine kinase, receptor, type 1
img HP TAS, OMIM ID: 256800
HumanNRAS4893neuroblastoma RAS viral (v-ras) oncogene homolog
img HP TAS, OMIM ID: 162900
HumanHRAS3265Harvey rat sarcoma viral oncogene homolog
img HP TAS, OMIM ID: 162900
HumanGLB12720galactosidase, beta 1
img HP RolledUp, OMIM ID: 253010
HumanGALNS2588galactosamine (N-acetyl)-6-sulfate sulfatase
img HP RolledUp, OMIM ID: 253000
HumanFGFR32261fibroblast growth factor receptor 3
img HP TAS, OMIM ID: 162900
HumanDLX31747distal-less homeobox 3
img HP TAS, OMIM ID: 190320
HumanRUNX2860runt-related transcription factor 2
img HP TAS, OMIM ID: 156510
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011073Abnormality of dental color0self