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Disease Ontology (DO): pituitary 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:   pituitary gland disease [DOID:53] <6>(1|1) (1|0|0)
- 1:   hypopituitarism [DOID:9406] <4>(1|1) (1|0|0)
- 1:   hyperpituitarism [DOID:2444] <2>(0|0) (0|0|0)
- 1:   necrosis of pituitary [DOID:3646] <1>(0|0) (0|0|0)
- 1:   empty sella syndrome [DOID:3642](0|0) (0|0|0)
- 1:   inappropriate ADH syndrome [DOID:3401](0|0) (0|0|0)
- 1:   pituitary hypoplasia [DOID:7378](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain-like0.0005741Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Homeodomain0.0002498Direct


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)
Homeodomain-like0.0003525Direct


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