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Details
Link-It Detail - Human Phenotype - Abnormality of the nasopharynx
Debug Stats
  • ### Total Build Time: 34 ms 26.288 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 205 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=4 ms Completed: 4 ms rowSize= 773 bytes
  • CONCEPT_CHILDREN gt=2 ms Completed: 2 ms rowSize= 1.118 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.087 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=16 ms Completed: 16 ms rowSize= 20.959 KB
  • CONCEPT_XREFS gt=6 ms Completed: 6 ms rowSize= 1.024 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the nasopharynx HP:0001739
Parents (2)
img Abnormality of the pharynx HP:0000600
img Abnormality of the nose HP:0000366
Children (3)
img Recurrent upper respiratory tract infections HP:0002788
img Neoplasia of the nasopharynx HP:0100630
img Frequent upper respiratory tract infections HP:0001740
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the pharynx HP:0000600
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nose HP:0000366
Genes (103)

Species:
human : 103
Page Size
Current 25
  Page 1 of 5
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDIP100188011interstitial pneumonitis, desquamative, familial
img HP RolledUp, OMIM ID: 263000
HumanRSPH4A345895radial spoke head 4 homolog A (Chlamydomonas)
img HP RolledUp, OMIM ID: 612649
HumanNPCA1257641Nasopharyngeal carcinoma 1
img HP RolledUp, OMIM ID: 607107
HumanHGSNAT138050heparan-alpha-glucosaminide N-acetyltransferase
img HP RolledUp, OMIM ID: 252930
HumanDNAAF1123872dynein, axonemal, assembly factor 1
img HP RolledUp, OMIM ID: 613193
HumanTNFRSF13C115650tumor necrosis factor receptor superfamily, member 13C
img HP RolledUp, OMIM ID: 613494
HumanCCDC11493233coiled-coil domain containing 114
img HP RolledUp, OMIM ID: 615067
HumanDOCK881704dedicator of cytokinesis 8
HumanITPKC80271inositol-trisphosphate 3-kinase C
img HP RolledUp, OMIM ID: 611775
HumanGNPTAB79158N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
HumanCMDR64588Craniometaphyseal dysplasia, autosomal recessive
img HP IEA, OMIM ID: 218400
HumanDNAI264446dynein, axonemal, intermediate chain 2
img HP RolledUp, OMIM ID: 612444
HumanDCLRE1C64421DNA cross-link repair 1C
img HP IEA, OMIM ID: 602450
HumanRFMN57788Roifman syndrome
img HP IEA, OMIM ID: 300258
HumanAICDA57379activation-induced cytidine deaminase
HumanSALL457167sal-like 4 (Drosophila)
img HP IEA, OMIM ID: 607323
HumanLRRC8A56262leucine rich repeat containing 8 family, member A
img HP RolledUp, OMIM ID: 601495
HumanANKH56172ANKH inorganic pyrophosphate transport regulator
img HP IEA, OMIM ID: 123000
HumanDNAAF255172dynein, axonemal, assembly factor 2
img HP RolledUp, OMIM ID: 612518
HumanHEATR254919HEAT repeat containing 2
img HP RolledUp, OMIM ID: 614874
HumanHYDIN54768HYDIN, axonemal central pair apparatus protein
HumanNME851314NME/NM23 family member 8
img HP RolledUp, OMIM ID: 610852
HumanIL21R50615interleukin 21 receptor
img HP RolledUp, OMIM ID: 615207
HumanICOS29851inducible T-cell co-stimulator
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001739Abnormality of the nasopharynx0self