SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Primary gonadal insufficiency

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term (+ for parents, - for children) HP term [HP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the endocrine system [HP:0000818] <16>(30|34) (35|12|5)
+ 1:   Puberty and gonadal disorders [HP:0008373] <13>(17|18) (20|3|1)
0:   Primary gonadal insufficiency [HP:0008193](1|1) (1|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
NagB/RpiA/CoA transferase-like0.00008539Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
IF2B-like0Direct


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)
NagB/RpiA/CoA transferase-like0.00004074Direct


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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