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Mammalian Phenotype (MP): muscle degeneration

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Root: MP Hierarchy (mammalian/mouse phenotype from MGI_4.41)

Shortest distance to current term (+ for parents, - for children) MP term [MP ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + 3:   mammalian phenotype [MP:0000001] <29>
+ + 2:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ 1:   abnormal muscle morphology [MP:0002108] <16>(28|31) (31|22|21)
0:   muscle degeneration [MP:0000749] <2>(1|1) (1|0|0)
- 1:   skeletal muscle degeneration [MP:0009415] <1>(0|0) (0|0|0)
- 1:   cardiac muscle degeneration [MP:0009416](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
WW domain0.0007166Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
WW domain0.0004881Direct


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)
WW domain0.0003842Direct


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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