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Phenotypic Abnormality (PA): Hepatosplenomegaly

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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:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + + 3:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
+ + + 3:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Abnormality of the lymphatic system [HP:0100763] <7>(9|19) (15|8|5)
+ + 2:   Abnormality of the spleen [HP:0001743] <2>(7|14) (9|4|3)
+ + 2:   Abnormality of the liver [HP:0001392] <4>(17|12) (17|7|0)
+ + 2:   Abnormality of abdomen morphology [HP:0001438] <7>(6|10) (8|5|2)
+ 1:   Abnormal liver morphology [HP:0410042] <25>(13|9) (13|4|0)
+ 1:   Abnormal spleen morphology [HP:0025408] <11>(7|13) (9|4|3)
+ 1:   Visceromegaly [HP:0003271] <3>(6|10) (8|5|2)
0:   Hepatosplenomegaly [HP:0001433](0|0) (0|0|0)