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Phenotypic Abnormality (PA): Aplasia/Hypoplasia affecting the anterior segment of the eye

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the eye [HP:0000478] <2>(64|78) (69|38|28)
+ + 2:   Abnormal anterior eye segment morphology [HP:0004328] <8>(17|21) (19|15|14)
+ + 2:   Abnormal eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ 1:   Aplasia/Hypoplasia affecting the eye [HP:0008056] <5>(4|4) (4|1|0)
+ 1:   Ocular anterior segment dysgenesis [HP:0007700] <7>(1|2) (1|0|0)
0:   Aplasia/Hypoplasia affecting the anterior segment of the eye [HP:0008062] <3>(0|1) (0|0|0)
- 1:   Aplasia/Hypoplasia of the lens [HP:0008063] <4>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the iris [HP:0008053] <2>(0|0) (0|0|0)
- 1:   Anterior segment of eye aplasia [HP:0007779](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.0007514Direct


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