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Disease Ontology (DO): Charlevoix-Saguenay spastic ataxia

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Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term
(+ for parents, - for children)
DO term [DO ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + + 7:   disease [DOID:4] <8>
+ + + + + + 6:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + + 5:   nervous system disease [DOID:863] <11>(51|61) (54|28|13)
+ + + + 4:   central nervous system disease [DOID:331] <16>(33|44) (36|21|9)
+ + + 3:   neurodegenerative disease [DOID:1289] <21>(24|31) (26|17|7)
+ + 2:   hereditary ataxia [DOID:0050951] <5>(2|1) (2|1|0)
+ 1:   autosomal recessive cerebellar ataxia [DOID:0050950] <21>(2|1) (2|1|0)
0:   Charlevoix-Saguenay spastic ataxia [DOID:0050946](0|0) (0|0|0)