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Details
Link-It Detail - Human Phenotype - Abnormality of the frontal sinuses
Debug Stats
  • ### Total Build Time: 31 ms 20.312 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 209 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= 447 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.101 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 ms rowSize= 3.019 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=13 ms Completed: 13 ms rowSize= 14.380 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.028 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the frontal sinuses HP:0002687
Parents (1)
img Abnormality of the sinuses HP:0000245
Children (3)
img Prominent frontal sinuses HP:0005478
img Obliteration of frontal sinuses HP:0005452
img Aplasia/Hypoplasia of the frontal sinuses HP:0009119
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of the sinuses HP:0000245
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the sinuses HP:0000245
img All HP:0000001img Phenotypic abnormality HP:00001189img Abnormality of the sinuses HP:0000245
Genes (17)

Species:
human : 17
SpeciesGeneGeneIdGene NameEvidence
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanAMER1139285APC membrane recruitment protein 1
img HP RolledUp, OMIM ID: 300373
HumanDNAI127019dynein, axonemal, intermediate chain 1
img HP RolledUp, OMIM ID: 244400
HumanDNAH118701dynein, axonemal, heavy chain 11
img HP RolledUp, OMIM ID: 244400
HumanNOTCH24853notch 2
img HP RolledUp, OMIM ID: 102500
HumanTRIM374591tripartite motif containing 37
img HP RolledUp, OMIM ID: 253250
HumanKCNJ23759potassium inwardly-rectifying channel, subfamily J, member 2
img HP RolledUp, OMIM ID: 170390
HumanFUCA12517fucosidase, alpha-L- 1, tissue
img HP RolledUp, OMIM ID: 230000
HumanFLNA2316filamin A, alpha
img HP TAS, OMIM ID: 311300
img HP TAS, OMIM ID: 305620
img HP TAS, OMIM ID: 304120
HumanDNAH51767dynein, axonemal, heavy chain 5
img HP RolledUp, OMIM ID: 244400
HumanDLX31747distal-less homeobox 3
img HP TAS, OMIM ID: 190320
HumanCTSK1513cathepsin K
img HP RolledUp, OMIM ID: 265800
HumanCOL11A11301collagen, type XI, alpha 1
img HP RolledUp, OMIM ID: 154780
HumanRUNX2860runt-related transcription factor 2
img HP RolledUp, OMIM ID: 119600
HumanATRX546alpha thalassemia/mental retardation syndrome X-linked
img HP RolledUp, OMIM ID: 301040
HumanALX3257ALX homeobox 3
img HP RolledUp, OMIM ID: 136760
HumanAGA175aspartylglucosaminidase
img HP RolledUp, OMIM ID: 208400
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002687Abnormality of the frontal sinuses0self