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Phenotypic Abnormality (PA): Small intestinal stenosis

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + + 4:   Abnormality of digestive system morphology [HP:0025033] <2>(13|19) (17|9|4)
+ + + + 4:   Abnormality of the gastrointestinal tract [HP:0011024] <3>(24|27) (28|14|4)
+ + + 3:   Morphological abnormality of the gastrointestinal tract [HP:0012718] <8>(13|19) (17|9|4)
+ + 2:   Abnormal intestine morphology [HP:0002242] <22>(8|11) (12|3|0)
+ 1:   Abnormality of the small intestine [HP:0002244] <16>(1|2) (2|0|0)
0:   Small intestinal stenosis [HP:0012848] <1>(0|1) (0|0|0)
- 1:   Duodenal stenosis [HP:0100867](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
RecA protein-like (ATPase-domain)0.000001382Direct


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