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Phenotypic Abnormality (PA): Abnormal circulating progesterone level

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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:   Abnormal circulating hormone level [HP:0003117] <28>(4|9) (6|4|1)
+ 1:   Puberty and gonadal disorders [HP:0008373] <13>(17|18) (20|3|1)
0:   Abnormal circulating progesterone level [HP:0031212] <3>(1|1) (1|0|0)
- 1:   Decreased circulating progesterone [HP:0008233](0|0) (0|0|0)
- 1:   Elevated circulating 17-hydroxyprogesterone [HP:0031213](0|0) (0|0|0)
- 1:   Increased circulating progesterone [HP:0031216](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
NagB/RpiA/CoA transferase-like0.0000002155Direct


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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
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Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
NagB/RpiA/CoA transferase-like0.0000000886Direct


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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