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Phenotypic Abnormality (PA): Polydipsia

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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:   Behavioral abnormality [HP:0000708] <38>(17|24) (19|15|5)
+ + 2:   Abnormal consumption behavior [HP:0040202] <2>(0|1) (0|1|0)
+ 1:   Abnormal drinking behavior [HP:0030082] <2>(0|1) (0|1|0)
0:   Polydipsia [HP:0001959](0|1) (0|1|0)


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
Cytoplasmic domain of inward rectifier potassium channel0.00002056Direct


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

Supra-domain (including individual superfamily)

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
81324,81296
  • 81324 - Voltage-gated potassium channels
  • 81296 - E set domains
  • 0.00001304Direct