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Details
Link-It Detail - Human Phenotype - Abnormality of the lacrimal duct
Debug Stats
  • ### Total Build Time: 40 ms 21.616 KB
  • CONCEPT_NAME gt=12 ms Completed: 12 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 299 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=4 ms Completed: 4 ms rowSize= 459 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.716 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=6 ms Completed: 6 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=12 ms Completed: 12 ms rowSize= 15.674 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the lacrimal duct HP:0011481
Definition (1)
An abnormality of the ` lacrimal duct` (FMA:61063), a duct that drain tears from the conjunctiva, via the lacrimal puncta, into the lacrimal sac.
Parents (1)
img Abnormality of the nasolacrimal system HP:0000614
Children (5)
img Hypoplastic lacrimal duct HP:0007900
img Lacrimal duct atresia HP:0000564
img Lacrimal duct aplasia HP:0007925
img Malformed lacrimal ducts HP:0007993
img Nasolacrimal duct obstruction HP:0000579
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the nasolacrimal system HP:0000614
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the nasolacrimal system HP:0000614
Genes (19)

Species:
human : 19
SpeciesGeneGeneIdGene NameEvidence
HumanHPPD100682260Hypertelorism, preauricular sinus, punctal pits, and deafness
img HP RolledUp, OMIM ID: 614187
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanFREM2341640FRAS1 related extracellular matrix protein 2
img HP RolledUp, OMIM ID: 219000
HumanFREM1158326FRAS1 related extracellular matrix 1
img HP RolledUp, OMIM ID: 248450
HumanFRAS180144Fraser syndrome 1
img HP RolledUp, OMIM ID: 219000
HumanNHP255651NHP2 ribonucleoprotein
img HP RolledUp, OMIM ID: 224230
HumanNOP1055505NOP10 ribonucleoprotein
img HP RolledUp, OMIM ID: 224230
HumanGRIP123426glutamate receptor interacting protein 1
img HP RolledUp, OMIM ID: 219000
HumanTP638626tumor protein p63
img HP RolledUp, OMIM ID: 603543
img HP RolledUp, OMIM ID: 103285
img HP RolledUp, OMIM ID: 106260
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
img HP RolledUp, OMIM ID: 113620
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
HumanJBS3719Jacobsen syndrome
img HP RolledUp, OMIM ID: 147791
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
HumanEYA12138eyes absent homolog 1 (Drosophila)
img HP RolledUp, OMIM ID: 113650
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanCD151977CD151 molecule (Raph blood group)
img HP RolledUp, OMIM ID: 609057
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0011481Abnormality of the lacrimal duct0self