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

Mammalian Phenotype (MP): abnormal Wallerian degeneration

(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>
+ + + 3:   nervous system phenotype [MP:0003631] <2>(98|128) (113|79|50)
+ + 2:   abnormal nervous system physiology [MP:0003633] <38>(43|60) (52|31|18)
+ + 2:   homeostasis/metabolism phenotype [MP:0005376] <7>(140|174) (149|96|44)
+ 1:   abnormal neuron physiology [MP:0004811] <12>(8|12) (11|7|5)
+ 1:   abnormal response to injury [MP:0005164] <10>(12|22) (17|11|7)
0:   abnormal Wallerian degeneration [MP:0010653] <1>(0|0) (0|0|0)
- 1:   slow Wallerian degeneration [MP:0010654](0|0) (0|0|0)