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Details
Link-It Detail - Human Phenotype - Abnormality of the nasal mucosa
Debug Stats
  • ### Total Build Time: 21 ms 9.691 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 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=4 ms Completed: 4 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 768 bytes
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.159 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=6 ms Completed: 6 ms rowSize= 5.978 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.025 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the nasal mucosa HP:0000433
Parents (1)
img Abnormality of the nose HP:0000366
Children (2)
img Nasal polyposis HP:0100582
img Nasal mucosa telangiectasia HP:0000434
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nose HP:0000366
Genes (7)

Species:
human : 7
SpeciesGeneGeneIdGene NameEvidence
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
img HP RolledUp, OMIM ID: 610655
HumanTAPBP6892TAP binding protein (tapasin)
img HP RolledUp, OMIM ID: 604571
HumanTAP26891transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)
img HP RolledUp, OMIM ID: 604571
HumanTAP16890transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)
img HP RolledUp, OMIM ID: 604571
HumanENG2022endoglin
img HP RolledUp, OMIM ID: 187300
HumanECM11893extracellular matrix protein 1
img HP RolledUp, OMIM ID: 247100
HumanACVRL194activin A receptor type II-like 1
img HP RolledUp, OMIM ID: 600376
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000433Abnormality of the nasal mucosa0self