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Disease Ontology (DO): retinal disease

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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> (#SF|#FA) #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:   sensory system disease [DOID:0050155] <2>(16|13) (17|5|2)
+ + 2:   eye and adnexa disease [DOID:1492] <3>(13|11) (14|5|2)
+ 1:   eye disease [DOID:5614] <34>(13|11) (14|5|2)
0:   retinal disease [DOID:5679] <20>(3|1) (4|2|1)
- 1:   Leber congenital amaurosis [DOID:14791] <17>(0|0) (0|0|0)
- 1:   retinal degeneration [DOID:8466] <8>(2|1) (3|2|1)
- 1:   retinal vascular disease [DOID:2462] <4>(1|0) (1|0|0)
- 1:   night blindness [DOID:8499] <3>(0|0) (0|0|0)
- 1:   retinitis [DOID:3612] <3>(0|0) (0|1|0)
- 1:   chorioretinal scar [DOID:11086] <2>(0|0) (0|0|0)
- 1:   blindness [DOID:1432] <1>(0|0) (0|0|0)
- 1:   retinal detachment [DOID:5327] <1>(0|0) (0|0|0)
- 1:   retinal edema [DOID:6929] <1>(0|0) (0|0|0)
- 1:   angioid streaks [DOID:13401](0|0) (0|0|0)
- 1:   bradyopsia [DOID:0050335](0|0) (0|0|0)
- 1:   cone dystrophy [DOID:0050795](0|0) (0|0|0)
- 1:   enhanced S-cone syndrome [DOID:0090059](0|0) (0|0|0)
- 1:   hypertensive retinopathy [DOID:11561](0|0) (0|0|0)
- 1:   macular holes [DOID:7633](0|0) (0|0|0)
- 1:   nerve fibre bundle defect [DOID:5678](0|0) (0|0|0)
- 1:   proliferative vitreoretinopathy [DOID:9719](0|0) (0|0|0)
- 1:   retinal ischemia [DOID:12510](0|0) (0|0|0)
- 1:   retinopathy of prematurity [DOID:13025](0|0) (0|0|0)
- 1:   rubeosis iridis [DOID:14000](0|0) (0|0|0)


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Complement control module/SCR domain0.003898Inherited
TIMP-like0.1539Inherited
4-helical cytokines0.5392Inherited


Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Complement control module/SCR domain0.002629Inherited


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Complement control module/SCR domain0.002617Inherited
TIMP-like0.1247Inherited
Trypsin-like serine proteases0.1648Inherited
4-helical cytokines0.4765Inherited

(show details)
Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.000002198Direct
    49899,49899
  • 49899 - Concanavalin A-like lectins/glucanases
  • 49899 - Concanavalin A-like lectins/glucanases
  • 0.006378Inherited

    (show details)
    Supra-domain (Triple) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
    57535,57535,57535
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 57535 - Complement control module/SCR domain
  • 0.00000118Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)