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Mammalian Phenotype (MP): abnormal myotome development

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

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)
+ + + + + 5:   mammalian phenotype [MP:0000001] <29>
+ + + + 4:   muscle phenotype [MP:0005369] <2>(49|57) (54|37|28)
+ + + 3:   abnormal muscle morphology [MP:0002108] <16>(28|31) (31|22|21)
+ + 2:   abnormal muscle development [MP:0000733] <7>(1|2) (1|0|0)
+ 1:   abnormal myogenesis [MP:0000729] <4>(0|1) (0|0|0)
0:   abnormal myotome development [MP:0000737] <1>(0|1) (0|0|0)
- 1:   abnormal dermomyotome development [MP:0004206](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)
Paired domain0.000000161Direct


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