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Phenotypic Abnormality (PA): Craniofacial hyperostosis

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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|54|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)
+ + + 3:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + 2:   Hyperostosis [HP:0100774] <2>(0|0) (0|0|0)
+ + 2:   Abnormality of the calvaria [HP:0002683] <7>(8|15) (8|6|6)
+ + 2:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + 2:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ 1:   Abnormality of facial skeleton [HP:0011821] <14>(4|4) (5|6|9)
+ 1:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ 1:   Cranial hyperostosis [HP:0004437] <4>(0|0) (0|0|0)
0:   Craniofacial hyperostosis [HP:0004493] <1>(0|0) (0|0|0)
- 1:   Facial hyperostosis [HP:0005465] <2>(0|0) (0|0|0)