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Phenotypic Abnormality (PA): Exostoses

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + 2:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ 1:   Neoplasm of the skeletal system [HP:0010622] <10>(1|2) (2|1|0)
0:   Exostoses [HP:0100777] <7>(0|0) (0|0|0)
- 1:   Multiple exostoses [HP:0002762] <3>(0|0) (0|0|0)
- 1:   Exostoses of the forearm bones [HP:0003960] <2>(0|0) (0|0|0)
- 1:   Exostoses of hand bones [HP:0004276](0|0) (0|0|0)
- 1:   Exostosis of the external auditory canal [HP:0004459](0|0) (0|0|0)
- 1:   Pelvic bone exostoses [HP:0003276](0|0) (0|0|0)
- 1:   Rib exostoses [HP:0000896](0|0) (0|0|0)
- 1:   Scapular exostoses [HP:0000918](0|0) (0|0|0)