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Phenotypic Abnormality (PA): Gastroparesis

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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:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the gastrointestinal tract [HP:0011024] <3>(24|27) (28|14|4)
+ + + 3:   Abnormality of digestive system morphology [HP:0025033] <2>(13|19) (17|9|4)
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Morphological abnormality of the gastrointestinal tract [HP:0012718] <8>(13|19) (17|9|4)
+ 1:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ 1:   Abnormality of the stomach [HP:0002577] <13>(4|4) (5|2|0)
0:   Gastroparesis [HP:0002578](0|0) (0|0|0)