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Phenotypic Abnormality (PA): Orthostatic hypotension due to autonomic dysfunction

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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)
+ + + + + 5:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormal cardiovascular system physiology [HP:0011025] <16>(21|34) (29|18|16)
+ + + + 4:   Abnormality of the peripheral nervous system [HP:0410008] <3>(2|1) (2|2|0)
+ + + 3:   Abnormality of the autonomic nervous system [HP:0002270] <2>(2|1) (2|2|0)
+ + + 3:   Abnormal systemic blood pressure [HP:0030972] <4>(3|4) (3|3|5)
+ + 2:   Hypotension [HP:0002615] <4>(0|0) (0|1|0)
+ + 2:   Abnormal autonomic nervous system physiology [HP:0012332] <6>(2|0) (2|2|0)
+ 1:   Orthostatic hypotension [HP:0001278] <2>(0|0) (0|1|0)
0:   Orthostatic hypotension due to autonomic dysfunction [HP:0004926](0|0) (0|1|0)


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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)
48371,48371
  • 48371 - ARM repeat
  • 48371 - ARM repeat
  • 0.000001792Direct