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Phenotypic Abnormality (PA): Intercostal 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:   Abnormality of the skeletal system [HP:0000924] <7>(88|98) (93|54|34)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormality of skeletal morphology [HP:0011842] <17>(86|89) (90|52|33)
+ + + 3:   Abnormality of the respiratory system [HP:0002086] <3>(30|35) (38|24|21)
+ + 2:   Functional respiratory abnormality [HP:0002795] <27>(10|13) (13|7|4)
+ + 2:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + 2:   Abnormal axial skeleton morphology [HP:0009121] <6>(47|61) (51|30|26)
+ 1:   Respiratory insufficiency [HP:0002093] <8>(2|4) (3|1|0)
+ 1:   Abnormality of the thorax [HP:0000765] <12>(13|18) (14|8|7)
+ 1:   Muscle weakness [HP:0001324] <22>(13|14) (15|4|0)
0:   Intercostal muscle weakness [HP:0004878](0|0) (0|0|0)