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Phenotypic Abnormality (PA): Intestinal obstruction

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Abnormality of digestive system morphology [HP:0025033] <2>(13|19) (17|9|4)
+ + + 3:   Abnormality of digestive system physiology [HP:0025032] <5>(29|32) (37|14|1)
+ + + 3:   Abnormality of the gastrointestinal tract [HP:0011024] <3>(24|27) (28|14|4)
+ + 2:   Functional abnormality of the gastrointestinal tract [HP:0012719] <11>(10|11) (14|2|0)
+ + 2:   Morphological abnormality of the gastrointestinal tract [HP:0012718] <8>(13|19) (17|9|4)
+ 1:   Abnormal intestine morphology [HP:0002242] <22>(8|11) (12|3|0)
+ 1:   Gastrointestinal obstruction [HP:0004796] <3>(1|1) (1|0|0)
0:   Intestinal obstruction [HP:0005214] <3>(0|1) (0|0|0)
- 1:   Ileus [HP:0002595] <2>(0|0) (0|0|0)
- 1:   High intestinal obstruction [HP:0005250](0|0) (0|0|0)
- 1:   Neonatal intestinal obstruction [HP:0005234](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)
Transforming growth factor (TGF)-beta0.0008054Direct


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