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Phenotypic Abnormality (PA): Abnormality of bony orbit of skull

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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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + 2:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ 1:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ 1:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
0:   Abnormality of bony orbit of skull [HP:3000030] <2>(0|0) (0|0|0)
- 1:   Orbital craniosynostosis [HP:0005472](0|0) (0|0|0)
- 1:   Shallow orbits [HP:0000586](0|0) (0|0|0)