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Disease Ontology (DO): eating disorder

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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)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of mental health [DOID:150] <12>(23|30) (24|14|4)
+ + 2:   developmental disorder of mental health [DOID:0060037] <2>(8|8) (8|2|0)
+ 1:   specific developmental disorder [DOID:0060038] <12>(4|3) (4|0|0)
0:   eating disorder [DOID:8670] <4>(2|1) (2|0|0)
- 1:   anorexia nervosa [DOID:8689](1|0) (1|0|0)
- 1:   bulimia nervosa [DOID:12129](0|0) (0|0|0)
- 1:   pica disease [DOID:12128](0|0) (0|0|0)
- 1:   rumination disorder [DOID:11507](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Family A G protein-coupled receptor-like0.0000184Direct
4-helical cytokines0.01512Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Rhodopsin-like0.00006121Direct


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)
Family A G protein-coupled receptor-like0.00001023Direct
4-helical cytokines0.01072Inherited


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