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Details
Link-It Detail - Human Phenotype - Abnormality of dental morphology
Debug Stats
  • ### Total Build Time: 25 ms 31.224 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 231 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= 445 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 4.565 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 23.465 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of dental morphology HP:0006482
Definition (1)
An abnormality of the `morphology` (PATO:0000051) of the `tooth` (FMA:12516).
Parents (1)
img Abnormality of the teeth HP:0000164
Children (14)
img Microdontia HP:0000691
img Abnormality of primary molar morphology HP:0006344
img Conical teeth HP:0000698
img Abnormality of the dental root HP:0006486
img Double tooth HP:0011089
img Shell teeth HP:0000694
img Microdontia of primary teeth HP:0006347
img Macrodontia HP:0001572
img Abnormality of premolar morphology HP:0011080
img Taurodontia HP:0000679
img Screwdriver-shaped incisors HP:0006346
img Misshapen teeth HP:0000697
img Abnormality of incisor morphology HP:0011063
img Abnormality of molar morphology HP:0011070
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (115)

Species:
human : 115
Page Size
Current 25
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP RolledUp, OMIM ID: 166750
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP TAS, OMIM ID: 608156
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP TAS, OMIM ID: 612582
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP TAS, OMIM ID: 612313
HumanSHFM3100049542Split-hand/foot malformation 3
img HP RolledUp, OMIM ID: 246560
HumanPTLS100038247Potocki-Lupski syndrome
img HP TAS, OMIM ID: 610883
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanZDHHC15158866zinc finger, DHHC-type containing 15
img HP RolledUp, OMIM ID: 300577
HumanVPS13B157680vacuolar protein sorting 13 homolog B (yeast)
img HP RolledUp, OMIM ID: 216550
HumanCCBE1147372collagen and calcium binding EGF domains 1
img HP TAS, OMIM ID: 235510
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanEVC2132884Ellis van Creveld syndrome 2
img HP RolledUp, OMIM ID: 225500
HumanEDARADD128178EDAR-associated death domain
img HP TAS, OMIM ID: 129490
img HP TAS, OMIM ID: 224900
HumanANTXR2118429anthrax toxin receptor 2
img HP TAS, OMIM ID: 236490
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP RolledUp, OMIM ID: 194050
HumanSCARF291179scavenger receptor class F, member 2
img HP TAS, OMIM ID: 600920
HumanADAMTS1081794ADAM metallopeptidase with thrombospondin type 1 motif, 10
img HP IEA, OMIM ID: 277600
HumanPVRL481607poliovirus receptor-related 4
img HP RolledUp, OMIM ID: 613573
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP TAS, OMIM ID: 257980
img HP RolledUp, OMIM ID: 150400
HumanPORCN64840porcupine homolog (Drosophila)
img HP TAS, OMIM ID: 305600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006482Abnormality of dental morphology0self