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Phenotypic Abnormality (PA): Abnormality of the peritoneum

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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 digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ 1:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
0:   Abnormality of the peritoneum [HP:0002585] <6>(0|0) (0|0|0)
- 1:   Peritonitis [HP:0002586] <1>(0|0) (0|0|0)
- 1:   Hemoperitoneum [HP:0011854](0|0) (0|0|0)
- 1:   Peritoneal abscess [HP:0100592](0|0) (0|0|0)
- 1:   Peritoneal effusion [HP:0030995](0|0) (0|0|0)
- 1:   Peritoneal mesothelioma [HP:0100003](0|0) (0|0|0)
- 1:   Retroperitoneal fibrosis [HP:0005200](0|0) (0|0|0)