SUPERFAMILY 1.75 HMM library and genome assignments server

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Disease Ontology (DO): premature ovarian failure

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

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:   reproductive system disease [DOID:15] <4>(11|13) (11|7|6)
+ + 2:   female reproductive system disease [DOID:229] <18>(7|11) (7|5|4)
+ 1:   ovarian disease [DOID:1100] <8>(0|2) (0|0|0)
0:   premature ovarian failure [DOID:5426](0|2) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Transforming growth factor (TGF)-beta0.0000005094Direct
Forkhead DNA-binding domain0.0001336Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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