dcGO - A comprehensive domain-centric ontology resource for post-genomic research on functions, phenotypes, diseases and more   
  
  

Phenotypic Abnormality (PA): Pancreatoblastoma

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Neoplasm [HP:0002664] <2>(20|21) (23|8|3)
+ + + 3:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
+ + 2:   Neoplasm by anatomical site [HP:0011793] <24>(18|19) (20|7|2)
+ + 2:   Abnormality of the pancreas [HP:0001732] <3>(6|5) (7|3|0)
+ 1:   Neoplasm of the pancreas [HP:0002894] <4>(2|2) (3|1|0)
0:   Pancreatoblastoma [HP:0100757](0|0) (0|0|0)