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Phenotypic Abnormality (PA): Periodic hypokalemic paresis

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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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Abnormality of central motor function [HP:0011442] <10>(22|26) (30|16|7)
+ + 2:   Paralysis [HP:0003470] <6>(4|3) (4|0|0)
+ 1:   Periodic paralysis [HP:0003768] <2>(1|0) (1|0|0)
0:   Periodic hypokalemic paresis [HP:0008153](1|0) (1|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Voltage-gated potassium channels0.00001487Direct


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)
Voltage-gated potassium channels0.000006363Direct


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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