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Phenotypic Abnormality (PA): Proteinuria

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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)
+ + + + + 5:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the urinary system [HP:0000079] <4>(38|41) (45|15|7)
+ + + 3:   Abnormality of the urinary system physiology [HP:0011277] <3>(23|26) (28|9|5)
+ + + 3:   Abnormality of metabolism/homeostasis [HP:0001939] <16>(75|82) (79|40|16)
+ + 2:   Abnormality of urine homeostasis [HP:0003110] <58>(17|20) (21|7|3)
+ 1:   Abnormal urine protein level [HP:0020129] <7>(0|1) (0|0|0)
0:   Proteinuria [HP:0000093] <5>(0|1) (0|0|0)
- 1:   Heavy proteinuria [HP:0012597](0|0) (0|0|0)
- 1:   Low-molecular-weight proteinuria [HP:0003126](0|0) (0|0|0)
- 1:   Mild proteinuria [HP:0012595](0|0) (0|0|0)
- 1:   Moderate proteinuria [HP:0012596](0|0) (0|0|0)
- 1:   Nephrotic range proteinuria [HP:0012593](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Noncollagenous (NC1) domain of collagen IV0.0003861Direct


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