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Details
Link-It Detail - Human Phenotype - Abnormality of primary teeth
Debug Stats
  • ### Total Build Time: 53 ms 29.160 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 205 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=4 ms Completed: 4 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=9 ms Completed: 9 ms rowSize= 2.720 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=17 ms Completed: 17 ms rowSize= 1.160 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 23.280 KB
  • CONCEPT_XREFS gt=3 ms Completed: 3 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of primary teeth HP:0006481
Definition (1)
Any abnormality of the `primary tooth` (FMA:55655).
Parents (1)
img Abnormality of the teeth HP:0000164
Children (8)
img Widely spaced primary teeth HP:0006313
img Abnormality of primary molar morphology HP:0006344
img Premature loss of primary teeth HP:0006323
img Small deciduous teeth HP:0006318
img Hypoplasia of the primary teeth HP:0006334
img Microdontia of primary teeth HP:0006347
img Persistence of primary teeth HP:0006335
img Delayed eruption of primary teeth HP:0000680
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (29)

Species:
human : 29
Page Size
Current 25
  Page 1 of 2
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanEDS8791254Ehlers-Danlos syndrome, type VIII
img HP RolledUp, OMIM ID: 130080
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanEDARADD128178EDAR-associated death domain
img HP RolledUp, OMIM ID: 129490
img HP RolledUp, OMIM ID: 224900
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP RolledUp, OMIM ID: 224750
img HP PCS, OMIM ID: 257980
HumanEHMT179813euchromatic histone-lysine N-methyltransferase 1
img HP RolledUp, OMIM ID: 610253
HumanFERMT155612fermitin family member 1
img HP RolledUp, OMIM ID: 173650
HumanBCOR54880BCL6 corepressor
img HP RolledUp, OMIM ID: 300166
HumanRAB2351715RAB23, member RAS oncogene family
img HP RolledUp, OMIM ID: 201000
HumanEDAR10913ectodysplasin A receptor
img HP RolledUp, OMIM ID: 224900
img HP RolledUp, OMIM ID: 129490
HumanFIG49896FIG4 homolog, SAC1 lipid phosphatase domain containing (S. cerevisiae)
img HP RolledUp, OMIM ID: 216340
HumanADAMTS29509ADAM metallopeptidase with thrombospondin type 1 motif, 2
img HP RolledUp, OMIM ID: 225410
HumanTNFSF118600tumor necrosis factor (ligand) superfamily, member 11
img HP RolledUp, OMIM ID: 259710
HumanVDR7421vitamin D (1,25- dihydroxyvitamin D3) receptor
img HP RolledUp, OMIM ID: 277440
HumanSTAT36774signal transducer and activator of transcription 3 (acute-phase response factor)
img HP RolledUp, OMIM ID: 147060
HumanPTH1R5745parathyroid hormone 1 receptor
img HP RolledUp, OMIM ID: 125350
HumanMSX14487msh homeobox 1
img HP RolledUp, OMIM ID: 189500
HumanKCNJ23759potassium inwardly-rectifying channel, subfamily J, member 2
img HP RolledUp, OMIM ID: 170390
HumanFLNA2316filamin A, alpha
img HP RolledUp, OMIM ID: 305620
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
HumanERCC62074excision repair cross-complementing rodent repair deficiency, complementation group 6
img HP RolledUp, OMIM ID: 133540
HumanCTSK1513cathepsin K
img HP RolledUp, OMIM ID: 265800
HumanCOL3A11281collagen, type III, alpha 1
img HP RolledUp, OMIM ID: 130050
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006481Abnormality of primary teeth0self