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Phenotypic Abnormality (PA): Visual field defect

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the eye [HP:0000478] <2>(63|76) (67|38|28)
+ + + 3:   Abnormal eye physiology [HP:0012373] <17>(33|46) (37|22|20)
+ + 2:   Abnormality of vision [HP:0000504] <15>(6|17) (10|8|8)
+ 1:   Visual impairment [HP:0000505] <4>(0|8) (3|6|7)
0:   Visual field defect [HP:0001123] <9>(0|4) (1|2|0)
- 1:   Scotoma [HP:0000575] <7>(0|1) (0|1|0)
- 1:   Constriction of peripheral visual field [HP:0001133] <5>(0|0) (0|0|0)
- 1:   Abnormal visual field test [HP:0030588] <4>(0|0) (0|0|0)
- 1:   Hemianopia [HP:0012377] <2>(0|1) (1|1|0)
- 1:   Altitudinal visual field defect [HP:0030531](0|0) (0|0|0)
- 1:   Blind-spot enlargment [HP:0030644](0|0) (0|0|0)
- 1:   Glaucomatous visual field defect [HP:0007854](0|0) (0|0|0)
- 1:   Large central visual field defect [HP:0001129](0|0) (0|0|0)
- 1:   Progressive visual field defects [HP:0007987](0|0) (0|0|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
DNA gyrase/MutL, second domain0.000001824Direct
DNA gyrase/MutL, N-terminal domain0.000001824Direct
G proteins0.01824Inherited
PDZ domain0.06493Inherited


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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
PDZ domain-like0.103Inherited

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
55874,54211
  • 55874 - ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
  • 54211 - Ribosomal protein S5 domain 2-like
  • 0.000001423Direct
    50156,50156
  • 50156 - PDZ domain-like
  • 50156 - PDZ domain-like
  • 0.00941Inherited


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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