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Details
Link-It Detail - Human Phenotype - Abnormality of the nasolacrimal system
Debug Stats
  • ### Total Build Time: 30 ms 31.966 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 213 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 288 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=3 ms Completed: 3 ms rowSize= 466 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 3.330 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=3 ms Completed: 3 ms rowSize= 2.127 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=18 ms Completed: 18 ms rowSize= 24.388 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.032 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the nasolacrimal system HP:0000614
Definition (1)
An abnormality of the nasolacrimal drainage system, which serves as a conduit for tear flow from the external eye to the nasal cavity.
Parents (1)
img Abnormality of tear glands or tear production HP:0000521
Children (10)
img Nasolacrimal duct obstruction HP:0000579
img Absent lacrimal puncta HP:0001092
img Abnormality of the lacrimal duct HP:0011481
img Ectopic lacrimal punctum HP:0010748
img Hypoplastic lacrimal duct HP:0007900
img Lacrimal duct atresia HP:0000564
img Lacrimal duct aplasia HP:0007925
img Abnormality of the lacrimal punctum HP:0011479
img Dacrocystitis HP:0000620
img Abnormality of the lacrimal gland HP:0011482
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of tear glands or tear production HP:0000521
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of tear glands or tear production HP:0000521
Genes (27)

Species:
human : 27
Page Size
Current 25
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Current 1
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
HumanUBR1197131ubiquitin protein ligase E3 component n-recognin 1
img HP RolledUp, OMIM ID: 243800
HumanFREM1158326FRAS1 related extracellular matrix 1
img HP RolledUp, OMIM ID: 248450
HumanFRAS180144Fraser syndrome 1
img HP RolledUp, OMIM ID: 219000
HumanNOD264127nucleotide-binding oligomerization domain containing 2
img HP RolledUp, OMIM ID: 181000
HumanBTNL256244butyrophilin-like 2 (MHC class II associated)
img HP RolledUp, OMIM ID: 181000
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: 604292
img HP RolledUp, OMIM ID: 129400
img HP RolledUp, OMIM ID: 103285
img HP RolledUp, OMIM ID: 106260
img HP RolledUp, OMIM ID: 603543
HumanWHSC17468Wolf-Hirschhorn syndrome candidate 1
img HP TAS, OMIM ID: 194190
HumanWHCR7467Wolf-Hirschhorn syndrome chromosome region
img HP TAS, OMIM ID: 194190
HumanTWIST17291twist basic helix-loop-helix transcription factor 1
img HP IEA, OMIM ID: 101400
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
img HP RolledUp, OMIM ID: 113620
HumanTCOF16949Treacher Collins-Franceschetti syndrome 1
img HP RolledUp, OMIM ID: 154500
HumanJBS3719Jacobsen syndrome
img HP RolledUp, OMIM ID: 147791
HumanHLA-DRB13123
img HP RolledUp, OMIM ID: 181000
HumanFGFR22263fibroblast growth factor receptor 2
img HP IEA, OMIM ID: 101400
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: 180920
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
HumanEEC11913ectrodactyly, ectodermal dysplasia and cleft lip/palate syndrome 1
img HP RolledUp, OMIM ID: 129900
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000614Abnormality of the nasolacrimal system0self