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Details
Link-It Detail - Human Phenotype - Abnormality of refraction
Debug Stats
  • ### Total Build Time: 42 ms 27.991 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 200 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=5 ms Completed: 5 ms rowSize= 443 bytes
  • CONCEPT_CHILDREN gt=12 ms Completed: 12 ms rowSize= 1.035 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.082 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=23 ms Completed: 23 ms rowSize= 23.082 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of refraction HP:0000539
Parents (1)
img Abnormality of the eye HP:0000478
Children (3)
img Myopia HP:0000545
img Hypermetropia HP:0000540
img Astigmatism HP:0000483
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the eye HP:0000478
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the eye HP:0000478
Genes (256)

Species:
human : 256
Page Size
Current 25
  Page 1 of 11
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanDEL17Q12100884130Chromosome 17q12 deletion syndrome
img HP RolledUp, OMIM ID: 614527
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMYP19100653370Myopia 19, autosomal dominant
img HP RolledUp, OMIM ID: 613969
HumanBED100653365Bornholm eye disease
img HP RolledUp, OMIM ID: 300843
HumanLCR-OPSIN100534624
img HP RolledUp, OMIM ID: 303700
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanAMMEC100499260Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
img HP RolledUp, OMIM ID: 300194
HumanDUP5P13100379202Chromosome 5p13 duplication syndrome
img HP RolledUp, OMIM ID: 613174
HumanMYP18100359406myopia 18 (high grade, autosomal recessive)
img HP RolledUp, OMIM ID: 255500
HumanMYP17100359401myopia 17
img HP RolledUp, OMIM ID: 608367
HumanSPG45100322879spastic paraplegia 45 (autosomal recessive)
img HP RolledUp, OMIM ID: 613162
HumanMYP15100294716myopia 15
img HP RolledUp, OMIM ID: 612717
HumanDEL6PTER100270803Chromosome 6pter deletion syndrome
img HP RolledUp, OMIM ID: 612582
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL1Q21100217370Chromosome 1q21.1 deletion syndrome
img HP RolledUp, OMIM ID: 612474
HumanRSTSS100188814Chromosome 16p13.3 deletion syndrome
img HP RolledUp, OMIM ID: 610543
HumanAUTS14100187724autism, susceptibility to, 14
img HP RolledUp, OMIM ID: 611913
HumanSHFM3100049542Split-hand/foot malformation 3
img HP RolledUp, OMIM ID: 246560
HumanPTLS100038247Potocki-Lupski syndrome
img HP RolledUp, OMIM ID: 610883
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000539Abnormality of refraction0self