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Phenotypic Abnormality (PA): Abnormal female reproductive system physiology

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + 2:   Abnormality of the genital system [HP:0000078] <3>(35|34) (37|10|3)
+ 1:   Abnormality of reproductive system physiology [HP:0000080] <5>(9|9) (11|3|2)
0:   Abnormal female reproductive system physiology [HP:0030012] <2>(1|1) (2|0|0)
- 1:   Female sexual dysfunction [HP:0030014] <5>(1|1) (2|0|0)
- 1:   Endometriosis [HP:0030127] <1>(0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Family A G protein-coupled receptor-like0.01265Inherited


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Rhodopsin-like0.008495Inherited


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)
Immunoglobulin0.007585Inherited
Family A G protein-coupled receptor-like0.008299Inherited


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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