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Phenotypic Abnormality (PA): Cranial asymmetry

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|55|34)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + 5:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + + 4:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ + + + 4:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormal skull morphology [HP:0000929] <14>(25|38) (28|22|20)
+ + 2:   Abnormality of the calvaria [HP:0002683] <7>(8|15) (8|6|6)
+ 1:   Abnormality of calvarial morphology [HP:0002648] <18>(3|9) (3|3|6)
0:   Cranial asymmetry [HP:0000267] <1>(0|1) (0|0|0)
- 1:   Craniofacial asymmetry [HP:0004484](0|0) (0|0|0)