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Phenotypic Abnormality (PA): Generalized amyotrophy

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + 3:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ + 2:   Abnormality of muscle size [HP:0030236] <3>(6|6) (6|3|0)
+ 1:   Skeletal muscle atrophy [HP:0003202] <12>(4|4) (4|2|0)
0:   Generalized amyotrophy [HP:0003700] <1>(0|0) (0|1|0)
- 1:   Generalized limb muscle atrophy [HP:0009055](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
  • 0.000006332Direct