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Phenotypic Abnormality (PA): Aplasia/Hypoplasia of the ear

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the ear [HP:0000598] <2>(17|32) (21|13|11)
+ 1:   Abnormal ear morphology [HP:0031703] <5>(15|26) (18|11|10)
0:   Aplasia/Hypoplasia of the ear [HP:0008771] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the external ear [HP:0008772] <3>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the inner ear [HP:0008774] <2>(0|0) (0|0|0)
- 1:   Aplasia/Hypoplasia of the middle ear [HP:0008773](0|0) (0|0|0)