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Phenotypic Abnormality (PA): Developmental cataract

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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>(64|78) (69|38|28)
+ + + 3:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ + 2:   Abnormality of the lens [HP:0000517] <6>(6|8) (7|9|10)
+ + 2:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|22) (19|15|14)
+ 1:   Cataract [HP:0000518] <11>(3|4) (3|3|2)
+ 1:   Ocular anterior segment dysgenesis [HP:0007700] <7>(1|2) (1|0|0)
0:   Developmental cataract [HP:0000519](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
gamma-Crystallin-like0.0000008645Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Crystallins/Ca-binding development proteins0.0000005194Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
gamma-Crystallin-like0.0000003424Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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