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Details
Link-It Detail - Human Phenotype - Abnormality of the external nose
Debug Stats
  • ### Total Build Time: 39 ms 26.005 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 207 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 204 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=3 ms Completed: 3 ms rowSize= 1.740 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=4 ms Completed: 4 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= 21.100 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.026 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the external nose HP:0010938
Definition (1)
An abnormality of the `external nose` (FMA:59515).
Parents (1)
img Abnormality of the nose HP:0000366
Children (5)
img Abnormality of the nasal tip HP:0000436
img Abnormality of the columella HP:0009929
img Abnormality of the nasal dorsum HP:0011119
img Abnormality of the nasal root HP:0000423
img Abnormality of the nasal alae HP:0000429
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of the nose HP:0000366
Genes (302)

Species:
human : 302
Page Size
Current 25
  Page 1 of 13
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanOTDD100885788Otodental dysplasia chromsome deletion syndrome
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanDEL17Q11.2100852404
img HP RolledUp, OMIM ID: 613675
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL3PTERP251006533853p- syndrome
img HP RolledUp, OMIM ID: 613792
HumanDEL13Q14100653382Chromosome 13q14 deletion syndrome
img HP RolledUp, OMIM ID: 613884
HumanDEL17P13.1100653374
img HP RolledUp, OMIM ID: 613776
HumanDEL1P32P31100532738Chromosome 1p32-p31 deletion syndrome
img HP RolledUp, OMIM ID: 613735
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
img HP RolledUp, OMIM ID: 612530
HumanDUP17Q21.31100529226
img HP RolledUp, OMIM ID: 613533
HumanDEL6Q11Q14100529221Chromosome 6q11-q14 deletion syndrome
img HP RolledUp, OMIM ID: 613544
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL16P12.1P11.2100526742
img HP RolledUp, OMIM ID: 613604
HumanOCLN100506658occludin
HumanDUP16P13.3100505393
img HP RolledUp, OMIM ID: 613458
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanLKMCD100302058Leukoencephalopathy with metaphyseal chondrodysplasia
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL9P100240748Chromosome 9p deletion syndrome
HumanDEL2P16.1-P15100240740
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0010938Abnormality of the external nose0self