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Details
Link-It Detail - Human Phenotype - Abnormal number of permanent teeth
Debug Stats
  • ### Total Build Time: 22 ms 11.209 KB
  • CONCEPT_NAME gt=5 ms Completed: 5 ms rowSize= 209 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 240 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=3 ms Completed: 3 ms rowSize= 450 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 1.161 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=5 ms Completed: 5 ms rowSize= 7.562 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormal number of permanent teeth HP:0011044
Definition (1)
The presence of an `altered number of`(PATO:0002083) of `permanent teeth` (FMA:55654).
Parents (1)
img Abnormal number of teeth HP:0006483
Children (1)
img Agenesis of permanent teeth HP:0006349
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormal number of teeth HP:0006483
Genes (9)

Species:
human : 9
SpeciesGeneGeneIdGene NameEvidence
HumanECTD8101101768Ectodermal dysplasia 8, hair/tooth/nail type
img HP RolledUp, OMIM ID: 602401
HumanKCTD1284252potassium channel tetramerization domain containing 1
img HP RolledUp, OMIM ID: 181270
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanWNT10A80326wingless-type MMTV integration site family, member 10A
img HP RolledUp, OMIM ID: 257980
HumanRAB2351715RAB23, member RAS oncogene family
img HP RolledUp, OMIM ID: 201000
HumanRECQL49401RecQ protein-like 4
img HP RolledUp, OMIM ID: 268400
HumanOFD18481oral-facial-digital syndrome 1
img HP RolledUp, OMIM ID: 311200
HumanMSX14487msh homeobox 1
img HP RolledUp, OMIM ID: 189500
HumanLRP54041low density lipoprotein receptor-related protein 5
img HP RolledUp, OMIM ID: 144750
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011044Abnormal number of permanent teeth0self