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Disease Ontology (DO): retinitis

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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)
+ + + + + + + 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:   sensory system disease [DOID:0050155] <2>(16|13) (17|5|2)
+ + + 3:   eye and adnexa disease [DOID:1492] <3>(13|11) (14|5|2)
+ + 2:   eye disease [DOID:5614] <34>(13|11) (14|5|2)
+ 1:   retinal disease [DOID:5679] <20>(3|1) (4|2|1)
0:   retinitis [DOID:3612] <3>(0|0) (0|1|0)
- 1:   Cytomegalovirus retinitis [DOID:0080160](0|0) (0|0|0)
- 1:   acute retinal necrosis syndrome [DOID:3611](0|0) (0|0|0)
- 1:   histoplasmosis retinitis [DOID:11316](0|0) (0|0|0)


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

Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
49899,49899
  • 49899 - Concanavalin A-like lectins/glucanases
  • 49899 - Concanavalin A-like lectins/glucanases
  • 0.00005501Direct