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Phenotypic Abnormality (PA): Pneumothorax

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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 respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + 2:   Abnormal respiratory system morphology [HP:0012252] <5>(20|25) (26|18|17)
+ 1:   Abnormal lung morphology [HP:0002088] <28>(11|18) (18|11|7)
0:   Pneumothorax [HP:0002107] <3>(0|1) (0|0|0)
- 1:   Spontaneous pneumothorax [HP:0002108] <1>(0|0) (0|0|0)
- 1:   Multiple bilateral pneumothoraces [HP:0005939](0|0) (0|0|0)
- 1:   Repeated pneumothoraces [HP:0006522](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
VWC domain0.0001791Direct


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