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Phenotypic Abnormality (PA): Deeply set eye

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

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 eye morphology [HP:0012372] <12>(39|48) (41|29|22)
+ 1:   Abnormality of globe location [HP:0100886] <6>(0|5) (1|1|0)
0:   Deeply set eye [HP:0000490](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
BCR-homology GTPase activation domain (BH-domain)0.0008745Direct


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