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Details
Link-It Detail - Human Phenotype - Abnormality of the incisor
Debug Stats
  • ### Total Build Time: 30 ms 32.258 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 201 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=6 ms Completed: 6 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 5.981 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 23.121 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the incisor HP:0000676
Definition (1)
An abnormality of the `Incisor tooth` (FMA:12823).
Parents (1)
img Abnormality of the teeth HP:0000164
Children (18)
img Widely-spaced maxillary central incisors HP:0001566
img Single central incisor HP:0001573
img Macrodontia of permanent maxillary central incisor HP:0000675
img Abnormally pointed upper lateral incisors HP:0006345
img Supernumerary maxillary incisor HP:0006332
img Agenesis of incisor HP:0006485
img Maxillary lateral incisor microdontia HP:0001593
img Conical mandibular incisor HP:0006339
img Shovel-shaped maxillary central incisors HP:0006358
img Central incisor gap HP:0001570
img Misalignment of incisors HP:0011062
img Screwdriver-shaped incisors HP:0006346
img Crowded maxillary incisors HP:0006333
img Peg-shaped incisors HP:0000673
img Rotated maxillary central incisors HP:0006330
img Discolored lateral incisors HP:0006290
img Abnormality of incisor morphology HP:0011063
img Abnormal number of incisors HP:0011064
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (26)

Species:
human : 26
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
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
HumanBCOR54880BCL6 corepressor
img HP RolledUp, OMIM ID: 309800
img HP RolledUp, OMIM ID: 300166
HumanANKRD1129123ankyrin repeat domain 11
img HP RolledUp, OMIM ID: 148050
HumanCHSY122856chondroitin sulfate synthase 1
img HP RolledUp, OMIM ID: 605282
HumanSNX38724sorting nexin 3
img HP RolledUp, OMIM ID: 601349
HumanIKBKG8517inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase gamma
img HP RolledUp, OMIM ID: 300640
HumanSIX36496SIX homeobox 3
img HP RolledUp, OMIM ID: 157170
HumanSHH6469sonic hedgehog
img HP RolledUp, OMIM ID: 142945
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
img HP RolledUp, OMIM ID: 309800
HumanGLI22736GLI family zinc finger 2
img HP RolledUp, OMIM ID: 610829
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
HumanEVC2121Ellis van Creveld syndrome
img HP RolledUp, OMIM ID: 193530
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanCOL11A11301collagen, type XI, alpha 1
img HP RolledUp, OMIM ID: 154780
HumanBLM641Bloom syndrome, RecQ helicase-like
img HP RolledUp, OMIM ID: 210900
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img HP RolledUp, OMIM ID: 301040
img HP RolledUp, OMIM ID: 309580
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000676Abnormality of the incisor0self