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

Phenotypic Abnormality (PA): Cerebellar hemisphere hypoplasia

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + + + 6:   Abnormality of brain morphology [HP:0012443] <13>(43|63) (53|34|15)
+ + + + + 5:   Abnormality of hindbrain morphology [HP:0011282] <2>(5|5) (7|2|1)
+ + + + + 5:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + + + 4:   Abnormality of the metencephalon [HP:0011283] <3>(5|5) (7|2|1)
+ + + + 4:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ + + 3:   Aplasia/Hypoplasia involving the central nervous system [HP:0002977] <13>(19|26) (23|13|3)
+ + + 3:   Abnormal cerebellum morphology [HP:0001317] <15>(5|5) (7|2|1)
+ + 2:   Aplasia/Hypoplasia of the cerebellum [HP:0007360] <2>(0|1) (1|1|0)
+ 1:   Cerebellar hypoplasia [HP:0001321] <2>(0|1) (1|1|0)
0:   Cerebellar hemisphere hypoplasia [HP:0100307](0|0) (0|0|0)