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Details
Link-It Detail - Human Phenotype - Abnormality of molar morphology
Debug Stats
  • ### Total Build Time: 18 ms 15.271 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 206 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
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=2 ms Completed: 2 ms rowSize= 776 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.098 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.092 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=7 ms Completed: 7 ms rowSize= 9.952 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of molar morphology HP:0011070
Parents (2)
img Abnormality of molar HP:0011077
img Abnormality of dental morphology HP:0006482
Children (3)
img Abnormality of primary molar morphology HP:0006344
img Mulberry molar HP:0011092
img Abnormality of permanent molar morphology HP:0011071
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of molar HP:0011077
img All HP:0000001img Phenotypic abnormality HP:000011810img Abnormality of dental morphology HP:0006482
Genes (15)

Species:
human : 15
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
HumanSMOC264094SPARC related modular calcium binding 2
img HP RolledUp, OMIM ID: 125400
HumanRAI110743retinoic acid induced 1
img HP RolledUp, OMIM ID: 182290
HumanADAMTS29509ADAM metallopeptidase with thrombospondin type 1 motif, 2
img HP RolledUp, OMIM ID: 225410
HumanKL9365klotho
HumanFGF238074fibroblast growth factor 23
HumanSOX106663SRY (sex determining region Y)-box 10
img HP RolledUp, OMIM ID: 601706
HumanOCRL4952oculocerebrorenal syndrome of Lowe
img HP RolledUp, OMIM ID: 309000
HumanGJA12697gap junction protein, alpha 1, 43kDa
HumanGALNT32591UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 3 (GalNAc-T3)
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
HumanEDA1896ectodysplasin A
HumanDLX31747distal-less homeobox 3
img HP RolledUp, OMIM ID: 104510
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011070Abnormality of molar morphology0self