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Details
Link-It Detail - Human Phenotype - Abnormality of dental enamel
Debug Stats
  • ### Total Build Time: 37 ms 30.019 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 203 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=5 ms Completed: 5 ms rowSize= 779 bytes
  • CONCEPT_CHILDREN gt=6 ms Completed: 6 ms rowSize= 3.321 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.094 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 22.278 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of dental enamel HP:0000682
Definition (1)
An abnormality of the `dental enamel` (FMA:55629).
Parents (2)
img Abnormality of the teeth HP:0000164
img Abnormality of dental structure HP:0011061
Children (10)
img Thin dental enamel HP:0003770
img Dental enamel pits HP:0009722
img Enamel dysplasia HP:0001565
img Yellow-brown discoloration of the teeth HP:0006286
img Grayish enamel HP:0000683
img Hypoplasia of dental enamel HP:0006297
img Hypomineralization of enamel HP:0006285
img Hypocalicifed-hypoplastic enamel HP:0006322
img Amelogenesis imperfecta HP:0000705
img Decreased enamel mineralisation HP:0006359
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of dental structure HP:0011061
Genes (95)

Species:
human : 95
Page Size
Current 25
  Page 1 of 4
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
img HP TAS, OMIM ID: 166750
HumanDEL17Q11.2100852404
img HP TAS, OMIM ID: 613675
HumanEDSS2100505394Ectodermal dysplasia-syndactyly syndrome 2
img HP RolledUp, OMIM ID: 613576
HumanSNORD116-1100033413
img HP TAS, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP TAS, OMIM ID: 176270
HumanDEL17Q21.31791085
img HP TAS, OMIM ID: 610443
HumanSNORD115-1338433
img HP TAS, OMIM ID: 176270
HumanFAM83H286077family with sequence similarity 83, member H
img HP RolledUp, OMIM ID: 130900
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP TAS, OMIM ID: 610443
HumanWDR72256764WD repeat domain 72
img HP RolledUp, OMIM ID: 613211
HumanC4orf26152816chromosome 4 open reading frame 26
img HP RolledUp, OMIM ID: 614832
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP TAS, OMIM ID: 176270
HumanWBSCR22114049Williams Beuren syndrome chromosome region 22
img HP TAS, OMIM ID: 194050
HumanPVRL481607poliovirus receptor-related 4
img HP RolledUp, OMIM ID: 613573
HumanROGDI79641rogdi homolog (Drosophila)
img HP TAS, OMIM ID: 226750
HumanPORCN64840porcupine homolog (Drosophila)
img HP TAS, OMIM ID: 305600
HumanFAM20C56975family with sequence similarity 20, member C
img HP RolledUp, OMIM ID: 259775
HumanTMEM16555858transmembrane protein 165
img HP RolledUp, OMIM ID: 614727
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanFERMT155612fermitin family member 1
img HP TAS, OMIM ID: 173650
HumanFAM20A54757family with sequence similarity 20, member A
img HP TAS, OMIM ID: 614253
HumanMAGEL254551MAGE-like 2
img HP TAS, OMIM ID: 176270
HumanMBTPS251360membrane-bound transcription factor peptidase, site 2
img HP TAS, OMIM ID: 308205
HumanMLXIPL51085MLX interacting protein-like
img HP TAS, OMIM ID: 194050
HumanANKRD1129123ankyrin repeat domain 11
img HP TAS, OMIM ID: 148050
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000682Abnormality of dental enamel0self