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Phenotypic Abnormality (PA): Muscle fiber inclusion bodies

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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 inclusion bodies [HP:0100299] <3>(3|2) (3|0|0)
- 1:   Muscle fiber cytoplasmatic inclusion bodies [HP:0100303] <5>(2|1) (2|0|0)
- 1:   Muscle fiber actin filament accumulation [HP:0025200](0|0) (0|0|0)
- 1:   Muscle fiber intranuclear inclusion bodies [HP:0100304](0|0) (0|0|0)


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

Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.00000929Direct
Kelch motif0.0001359Direct
POZ domain0.01027Inherited


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Tropomyosin0.000004317Direct
Kelch motif0.00006824Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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Jump to [ Top · Phenotype Hierarchy · Superfamily · Family · Supra-domain ]

Supra-domain (including individual superfamily)

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Supra-domain (Single) FDR (all) Annotation (direct or inherited)
Tropomyosin0.000003903Direct
Kelch motif0.00006362Direct
POZ domain0.006633Inherited


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
Plot tree as:   Download Newick format tree:
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