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Disease Ontology (DO): hyperandrogenism

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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)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + 3:   endocrine system disease [DOID:28] <7>(14|16) (15|4|1)
+ + 2:   gonadal disease [DOID:2277] <3>(2|3) (3|1|0)
+ 1:   sex differentiation disease [DOID:1923] <6>(2|2) (2|1|0)
0:   hyperandrogenism [DOID:11613](2|2) (2|1|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Insulin-like0.00000008696Direct
Cytochrome P4500.000249Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Insulin-like0.00000005184Direct
Phosphotyrosine-binding domain (PTB)0.00001974Direct


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)
Insulin-like0.00000004264Direct
Cytochrome P4500.00015Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
50729,50729
  • 50729 - PH domain-like
  • 50729 - PH domain-like
  • 0.00000647Direct


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