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Phenotypic Abnormality (PA): Intraalveolar nodular calcifications

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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>
+ + + 3:   Abnormality of the respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + 2:   Abnormal respiratory system morphology [HP:0012252] <5>(20|25) (26|18|17)
+ + 2:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ 1:   Ectopic calcification [HP:0010766] <26>(0|1) (1|1|0)
+ 1:   Abnormal lung morphology [HP:0002088] <28>(11|18) (18|11|7)
0:   Intraalveolar nodular calcifications [HP:0006514](0|0) (0|0|0)