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Details
Link-It Detail - Human Phenotype - Abnormality of incisor morphology
Debug Stats
  • ### Total Build Time: 20 ms 17.479 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 235 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=2 ms Completed: 2 ms rowSize= 782 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 2.671 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=5 ms Completed: 5 ms rowSize= 2.098 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 10.342 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of incisor morphology HP:0011063
Definition (1)
An abnormality of `morphology` (PATO:0000051) of the `incisor tooth` (FMA:12823).
Parents (2)
img Abnormality of the incisor HP:0000676
img Abnormality of dental morphology HP:0006482
Children (8)
img Conical incisor HP:0011065
img Dens in dente HP:0011088
img Maxillary lateral incisor microdontia HP:0001593
img Shovel-shaped maxillary central incisors HP:0006358
img Talon cusp HP:0011087
img Incisor macrodontia HP:0011081
img Screwdriver-shaped incisors HP:0006346
img Discolored lateral incisors HP:0006290
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of the incisor HP:0000676
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of dental morphology HP:0006482
Genes (14)

Species:
human : 14
SpeciesGeneGeneIdGene NameEvidence
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP RolledUp, OMIM ID: 235510
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP RolledUp, OMIM ID: 150400
HumanCHSY122856chondroitin sulfate synthase 1
img HP RolledUp, OMIM ID: 605282
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP RolledUp, OMIM ID: 300640
HumanSHH6469sonic hedgehog
HumanNHS4810Nance-Horan syndrome (congenital cataracts and dental anomalies)
img HP RolledUp, OMIM ID: 302350
HumanFGFR22263fibroblast growth factor receptor 2
img HP RolledUp, OMIM ID: 149730
HumanFGFR32261fibroblast growth factor receptor 3
img HP RolledUp, OMIM ID: 149730
HumanFGF102255fibroblast growth factor 10
img HP RolledUp, OMIM ID: 149730
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanCOL11A11301collagen, type XI, alpha 1
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011063Abnormality of incisor morphology0self