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

Disease Ontology (DO): autosomal recessive cerebellar ataxia

(show info)

Jump to [ Top · Hierarchy · Annotations ]

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)
+ + + + + + 6:   disease [DOID:4] <8>
+ + + + + 5:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + 4:   nervous system disease [DOID:863] <11>(51|61) (54|28|13)
+ + + 3:   central nervous system disease [DOID:331] <16>(33|44) (36|21|9)
+ + 2:   neurodegenerative disease [DOID:1289] <21>(24|31) (26|17|7)
+ 1:   hereditary ataxia [DOID:0050951] <5>(2|1) (2|1|0)
0:   autosomal recessive cerebellar ataxia [DOID:0050950] <21>(2|1) (2|1|0)
- 1:   Charlevoix-Saguenay spastic ataxia [DOID:0050946](0|0) (0|0|0)
- 1:   Friedreich ataxia [DOID:12705](0|0) (0|0|0)
- 1:   ataxia telangiectasia [DOID:12704](2|1) (2|1|0)
- 1:   ataxia with oculomotor apraxia type 1 [DOID:0050754](0|0) (0|0|0)
- 1:   ataxia with oculomotor apraxia type 2 [DOID:0050755](0|0) (0|0|0)
- 1:   ataxia with oculomotor apraxia type 3 [DOID:0060557](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 10 [DOID:0050999](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 11 [DOID:0080063](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 12 [DOID:0080060](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 13 [DOID:0080062](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 14 [DOID:0080058](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 15 [DOID:0080057](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 16 [DOID:0080029](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 17 [DOID:0080064](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 18 [DOID:0080042](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 19 [DOID:0080065](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 2 [DOID:0080061](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 20 [DOID:0080066](0|0) (0|0|0)
- 1:   autosomal recessive spinocerebellar ataxia 7 [DOID:0080059](0|0) (0|0|0)
- 1:   cerebellar ataxia, mental retardation and dysequlibrium syndrome [DOID:0050997](0|0) (0|0|0)
- 1:   infantile onset spinocerebellar ataxia [DOID:0050556](0|0) (0|0|0)

Superfamily

Jump to [ Top · Hierarchy ]

Superfamily

(show details)
SCOP term FDR (all) Annotation (direct or inherited)
SCOP hierarchy in SUPERFAMILY0.001114Inherited
Protein kinase-like (PK-like)0.1969Inherited

LINKTO: Domain2BO Download and Domain2BO Algorithm

Family

Jump to [ Top · Hierarchy ]

Family

(show details)
SCOP term FDR (all) Annotation (direct or inherited)
Phoshoinositide 3-kinase (PI3K), catalytic domain0.00000005872Direct

LINKTO: Domain2BO Download and Domain2BO Algorithm

Supra-domain (Single|Duplex|Triple)

Jump to [ Top · Hierarchy ]

Supra-domain (Single)

(
show details)
Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Protein kinase-like (PK-like)0.1623Inherited
ARM repeat0.2451Inherited

LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

Jump to [ Top · Hierarchy ]

Supra-domain (Duplex) in N- to C-terminal order

(
show details)
Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.000008516Direct

    LINKTO: Supra-domain2BO Download and Supra-domain2BO Algorithm

    Distribution on sTOL

    Plot distribution on species Tree Of Life (sTOL) for Superfamily and/or Family domains annotated by this DO term
    Plot tree as:   Download Newick format tree:
    (show help)
    Plot distribution on species Tree Of Life (sTOL) for single supra-domains annotated by this DO term
    Plot tree as:   Download Newick format tree:   Browsing in TREE OF LIFE:
    (show help)