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Phenotypic Abnormality (PA): Muscle fiber atrophy

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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>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
+ 1:   Abnormal muscle fiber morphology [HP:0004303] <25>(6|5) (6|2|0)
0:   Muscle fiber atrophy [HP:0100295] <2>(0|1) (0|0|0)
- 1:   Type 1 muscle fiber atrophy [HP:0011807](0|0) (0|0|0)
- 1:   Type 2 muscle fiber atrophy [HP:0003554](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Laminin-type module0.0001897Direct


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