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Details
Link-It Detail - Human Phenotype - Abnormality of the nasal septum
Debug Stats
  • ### Total Build Time: 40 ms 24.983 KB
  • CONCEPT_NAME gt=2 ms Completed: 1 ms rowSize= 206 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 203 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=6 ms Completed: 6 ms rowSize= 444 bytes
  • CONCEPT_CHILDREN gt=5 ms Completed: 5 ms rowSize= 2.352 KB
  • 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=24 ms Completed: 24 ms rowSize= 19.470 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 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 septum HP:0000419
Definition (1)
An abnormality of the `nasal septum` (FMA:54375).
Parents (1)
img Abnormality of the nose HP:0000366
Children (7)
img Deviated nasal septum HP:0004411
img Narrow nasal septum HP:0009936
img Abnormality of the columella HP:0009929
img Prominent nasal septum HP:0005322
img Short nasal septum HP:0000420
img Thick nasal septum HP:0009746
img Aplasia/Hypoplasia of the nasal septum HP:0009935
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nose HP:0000366
Genes (24)

Species:
human : 24
SpeciesGeneGeneIdGene NameEvidence
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanSRCAP10847Snf2-related CREBBP activator protein
img HP RolledUp, OMIM ID: 136140
HumanPQBP110084polyglutamine binding protein 1
img HP RolledUp, OMIM ID: 309500
HumanZEB29839zinc finger E-box binding homeobox 2
img HP RolledUp, OMIM ID: 235730
HumanHDAC49759histone deacetylase 4
img HP RolledUp, OMIM ID: 600430
HumanNOG9241noggin
img HP RolledUp, OMIM ID: 184460
img HP RolledUp, OMIM ID: 186500
HumanNAA108260N(alpha)-acetyltransferase 10, NatA catalytic subunit
img HP RolledUp, OMIM ID: 300855
HumanKDM6A7403lysine (K)-specific demethylase 6A
img HP RolledUp, OMIM ID: 300867
HumanTGIF17050TGFB-induced factor homeobox 1
img HP RolledUp, OMIM ID: 142946
HumanTFAP2A7020transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
img HP RolledUp, OMIM ID: 113620
HumanSIX36496SIX homeobox 3
img HP RolledUp, OMIM ID: 157170
HumanRPS6KA36197ribosomal protein S6 kinase, 90kDa, polypeptide 3
img HP RolledUp, OMIM ID: 303600
HumanPTCH15727patched 1
img HP RolledUp, OMIM ID: 610828
HumanMGAT24247mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
img HP RolledUp, OMIM ID: 212066
HumanJBS3719Jacobsen syndrome
img HP RolledUp, OMIM ID: 147791
HumanFLNB2317filamin B, beta
img HP RolledUp, OMIM ID: 112310
HumanEP3002033E1A binding protein p300
img HP RolledUp, OMIM ID: 180849
HumanCREBBP1387CREB binding protein
img HP RolledUp, OMIM ID: 180849
HumanBDMR626brachydactyly-mental retardation syndrome
img HP RolledUp, OMIM ID: 600430
HumanARSE415arylsulfatase E (chondrodysplasia punctata 1)
img HP RolledUp, OMIM ID: 302950
HumanALX3257ALX homeobox 3
img HP RolledUp, OMIM ID: 136760
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000419Abnormality of the nasal septum0self