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Details
Link-It Detail - Human Phenotype - Abnormal number of incisors
Debug Stats
  • ### Total Build Time: 27 ms 13.822 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 202 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 243 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=5 ms Completed: 5 ms rowSize= 774 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.085 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.090 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 8.291 KB
  • CONCEPT_XREFS gt=1 ms Completed: 0 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal number of incisors HP:0011064
Definition (1)
The presence of an `altered number of`(PATO:0002083) of the `incisor teeth` (FMA:12823)..
Parents (2)
img Abnormal number of teeth HP:0006483
img Abnormality of the incisor HP:0000676
Children (3)
img Supernumerary maxillary incisor HP:0006332
img Agenesis of incisor HP:0006485
img Single median maxillary incisor HP:0006315
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormal number of teeth HP:0006483
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the incisor HP:0000676
Genes (12)

Species:
human : 12
SpeciesGeneGeneIdGene NameEvidence
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
HumanBCOR54880BCL6 corepressor
img HP RolledUp, OMIM ID: 300166
HumanSIX36496SIX homeobox 3
img HP RolledUp, OMIM ID: 157170
HumanSHH6469sonic hedgehog
img HP RolledUp, OMIM ID: 147250
HumanPTCH15727patched 1
img HP RolledUp, OMIM ID: 610828
HumanNHS4810Nance-Horan syndrome (congenital cataracts and dental anomalies)
img HP RolledUp, OMIM ID: 302350
HumanMAA4080microphthalmia or anophthalmia and associated anomalies
HumanGLI22736GLI family zinc finger 2
img HP RolledUp, OMIM ID: 610829
HumanEVC2121Ellis van Creveld syndrome
img HP RolledUp, OMIM ID: 193530
HumanBLM641Bloom syndrome, RecQ helicase-like
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011064Abnormal number of incisors0self