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Phenotypic Abnormality (PA): Oculomotor nerve palsy

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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)
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormal eye physiology [HP:0012373] <17>(34|47) (37|22|20)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + 2:   Abnormality of eye movement [HP:0000496] <14>(8|15) (9|4|1)
+ + 2:   Abnormal peripheral nervous system morphology [HP:0000759] <14>(14|17) (18|6|0)
+ 1:   Abnormal cranial nerve morphology [HP:0001291] <10>(2|1) (2|1|0)
+ 1:   Ophthalmoparesis [HP:0000597] <5>(0|1) (0|1|0)
0:   Oculomotor nerve palsy [HP:0012246](0|0) (0|0|0)