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Phenotypic Abnormality (PA): Abnormal shape of the palpebral fissure

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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)
+ + + + + + + + + 9:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + + + 8:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + + 7:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + + 6:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + + 5:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ + + + 4:   Abnormality of the ocular adnexa [HP:0032039] <2>(17|24) (19|5|4)
+ + + 3:   Abnormal ocular adnexa morphology [HP:0030669] <6>(17|24) (19|5|4)
+ + 2:   Abnormal eyelid morphology [HP:0000492] <26>(10|17) (12|2|3)
+ 1:   Abnormality of the palpebral fissures [HP:0008050] <3>(4|8) (6|1|1)
0:   Abnormal shape of the palpebral fissure [HP:0200005] <2>(0|1) (0|0|0)
- 1:   Almond-shaped palpebral fissure [HP:0007874](0|0) (0|0|0)
- 1:   S-shaped palpebral fissures [HP:0007835](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)0.00018Direct


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