SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Infantile muscular hypotonia

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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>(62|74) (69|31|7)
+ + + 3:   Abnormal muscle physiology [HP:0011804] <12>(43|55) (52|22|4)
+ + 2:   Abnormal muscle tone [HP:0003808] <3>(21|33) (27|15|4)
+ 1:   Muscular hypotonia [HP:0001252] <9>(14|24) (17|9|4)
0:   Infantile muscular hypotonia [HP:0008947] <1>(1|1) (1|0|0)
- 1:   Infantile axial hypotonia [HP:0009062](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0002297Direct


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Family

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SCOP termFDR (all)Annotation (direct or inherited)
MIR domain0.0001047Direct


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)
MIR domain0.0001153Direct


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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