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Phenotypic Abnormality (PA): Respiratory insufficiency due to muscle weakness

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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)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormality of the respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + + 3:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + 2:   Functional respiratory abnormality [HP:0002795] <27>(10|13) (13|7|4)
+ + 2:   Muscle weakness [HP:0001324] <22>(13|14) (15|4|0)
+ 1:   Weakness of muscles of respiration [HP:0004347] <4>(1|0) (1|2|0)
+ 1:   Respiratory insufficiency [HP:0002093] <8>(2|4) (3|1|0)
0:   Respiratory insufficiency due to muscle weakness [HP:0002747] <1>(0|0) (0|1|0)
- 1:   Intermittent episodes of respiratory insufficiency due to muscle weakness [HP:0004889](0|0) (0|0|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)
53300,53300
  • 53300 - vWA-like
  • 53300 - vWA-like
  • 0.00001285Direct