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

Mammalian Phenotype (MP): abnormal blood-retinal barrier function

(show info)

Jump to [ Top · Hierarchy · Annotations ]

Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term
(+ for parents, - for children)
MP term [MP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   vision/eye phenotype [MP:0005391] <2>(43|53) (50|27|17)
+ 1:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ 1:   abnormal eye physiology [MP:0005253] <25>(8|9) (9|5|2)
0:   abnormal blood-retinal barrier function [MP:0014179](0|0) (0|0|0)