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Disease Ontology (DO): adrenal gland 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)
+ + + 3:   disease [DOID:4] <8>
+ + 2:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ 1:   endocrine system disease [DOID:28] <7>(14|16) (15|4|1)
0:   adrenal gland disease [DOID:9553] <5>(1|1) (1|0|0)
- 1:   adrenal cortex disease [DOID:3952] <4>(0|0) (0|0|0)
- 1:   Waterhouse-Friderichsen syndrome [DOID:9931](0|0) (0|0|0)
- 1:   congenital adrenal insufficiency [DOID:0050546](0|0) (0|0|0)
- 1:   corticosteroid-binding globulin deficiency [DOID:0090030](0|0) (0|0|0)
- 1:   medulloadrenal hyperfunction [DOID:12257](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Cytochrome P4500.0004295Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Cytochrome P4500.0001009Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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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)
Cytochrome P4500.0002623Direct


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