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Details
Link-It Detail - Human Phenotype - Abnormality of teeth spacing
Debug Stats
  • ### Total Build Time: 25 ms 27.289 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 203 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 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
  • CONCEPT_NAMESPACE gt=0 Completed: 0 ms rowSize= 168 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 445 bytes
  • CONCEPT_CHILDREN gt=1 ms Completed: 1 ms rowSize= 1.723 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=14 ms Completed: 14 ms rowSize= 22.442 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.022 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of teeth spacing HP:0006478
Namespace (1)
medical_genetics
Parents (1)
img Abnormality of the teeth HP:0000164
Children (5)
img Abnormal teeth spacing HP:0006303
img Crowded maxillary incisors HP:0006333
img Widely spaced teeth HP:0000687
img Irregularly spaced teeth HP:0006316
img Irregular, small, or absent incisors HP:0006340
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the teeth HP:0000164
Genes (37)

Species:
human : 37
Page Size
Current 25
  Page 1 of 2
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanKANSL1284058KAT8 regulatory NSL complex subunit 1
img HP RolledUp, OMIM ID: 610443
HumanIFT43112752intraflagellar transport 43 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 614099
HumanWDR3557539WD repeat domain 35
img HP RolledUp, OMIM ID: 613610
HumanMBD555777methyl-CpG binding domain protein 5
img HP RolledUp, OMIM ID: 156200
HumanIFT12255764intraflagellar transport 122 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 218330
HumanBCOR54880BCL6 corepressor
img HP RolledUp, OMIM ID: 309800
HumanVSX130813visual system homeobox 1
img HP RolledUp, OMIM ID: 122000
HumanNIPBL25836Nipped-B homolog (Drosophila)
img HP RolledUp, OMIM ID: 122470
HumanZEB29839zinc finger E-box binding homeobox 2
img HP RolledUp, OMIM ID: 235730
HumanPIGL9487phosphatidylinositol glycan anchor biosynthesis, class L
img HP RolledUp, OMIM ID: 280000
HumanCHST39469carbohydrate (chondroitin 6) sulfotransferase 3
img HP RolledUp, OMIM ID: 608637
img HP RolledUp, OMIM ID: 143095
HumanTP638626tumor protein p63
img HP RolledUp, OMIM ID: 106260
HumanUBE3A7337ubiquitin protein ligase E3A
img HP RolledUp, OMIM ID: 105830
HumanTCF46925transcription factor 4
img HP RolledUp, OMIM ID: 610954
HumanCDKL56792cyclin-dependent kinase-like 5
img HP RolledUp, OMIM ID: 105830
HumanSMARCA26595SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2
img HP RolledUp, OMIM ID: 601358
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img HP RolledUp, OMIM ID: 303600
HumanMECP24204methyl CpG binding protein 2 (Rett syndrome)
img HP RolledUp, OMIM ID: 105830
HumanMAN2B14125mannosidase, alpha, class 2B, member 1
img HP RolledUp, OMIM ID: 248500
HumanMAA4080microphthalmia or anophthalmia and associated anomalies
img HP RolledUp, OMIM ID: 309800
HumanIDS3423iduronate 2-sulfatase
img HP RolledUp, OMIM ID: 309900
HumanHMI3160hypomelanosis of Ito
img HP RolledUp, OMIM ID: 300337
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0006478Abnormality of teeth spacing0self