SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Stage 5 chronic kidney disease

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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)
+ + + + + + + 7:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + + 6:   Abnormality of the genitourinary system [HP:0000119] <5>(73|72) (80|28|9)
+ + + + + 5:   Abnormality of the urinary system [HP:0000079] <4>(38|41) (45|15|7)
+ + + + + 5:   Abnormality of the upper urinary tract [HP:0010935] <2>(21|22) (22|7|3)
+ + + + 4:   Abnormality of the urinary system physiology [HP:0011277] <3>(23|26) (28|9|5)
+ + + + 4:   Abnormality of the kidney [HP:0000077] <3>(17|16) (18|6|3)
+ + + 3:   Abnormal renal physiology [HP:0012211] <15>(9|10) (10|3|1)
+ + 2:   Renal insufficiency [HP:0000083] <3>(2|3) (2|2|1)
+ 1:   Chronic kidney disease [HP:0012622] <5>(0|1) (0|1|0)
0:   Stage 5 chronic kidney disease [HP:0003774](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Noncollagenous (NC1) domain of collagen IV0.00001089Direct


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Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
56436,56436
  • 56436 - C-type lectin-like
  • 56436 - C-type lectin-like
  • 0.00004674Direct