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Details
Link-It Detail - Human Phenotype - Abnormality of oral frenula
Debug Stats
  • ### Total Build Time: 26 ms 17.507 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 202 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=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=5 ms Completed: 5 ms rowSize= 451 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.376 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.166 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=11 ms Completed: 11 ms rowSize= 13.161 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.021 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of oral frenula HP:0000190
Parents (1)
img Abnormality of the oral cavity HP:0000163
Children (4)
img Fibrous syngnathia HP:0009754
img Accessory oral frenulum HP:0000191
img Ankyloglossia HP:0010296
img Short lingual frenulum HP:0000200
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the oral cavity HP:0000163
Genes (16)

Species:
human : 16
SpeciesGeneGeneIdGene NameEvidence
HumanCATMANS100862706Catel-Manzke syndrome
img HP RolledUp, OMIM ID: 302380
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
img HP RolledUp, OMIM ID: 611867
HumanB3GALTL145173beta 1,3-galactosyltransferase-like
img HP RolledUp, OMIM ID: 261540
HumanFAM111A63901family with sequence similarity 111, member A
img HP RolledUp, OMIM ID: 602361
HumanFERMT155612fermitin family member 1
img HP RolledUp, OMIM ID: 173650
HumanODPF54114Osseous dysplasia, digital, with facial pigmentary defects and multiple frenula
img HP IEA, OMIM ID: 300244
HumanTBX2250945T-box 22
img HP RolledUp, OMIM ID: 303400
HumanTCTN326123tectonic family member 3
img HP RolledUp, OMIM ID: 258860
HumanCD9610225CD96 molecule
img HP RolledUp, OMIM ID: 211750
HumanOGS28221Opitz G syndrome, type II
img HP RolledUp, OMIM ID: 145410
HumanROR24920receptor tyrosine kinase-like orphan receptor 2
img HP RolledUp, OMIM ID: 268310
HumanMMP14312matrix metallopeptidase 1 (interstitial collagenase)
img HP RolledUp, OMIM ID: 226600
HumanIRF63664interferon regulatory factor 6
img HP RolledUp, OMIM ID: 119500
HumanFLNA2316filamin A, alpha
img HP IEA, OMIM ID: 300244
HumanCOL7A11294collagen, type VII, alpha 1
img HP RolledUp, OMIM ID: 226600
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000190Abnormality of oral frenula0self