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Phenotypic Abnormality (PA): Limb-girdle muscle 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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of the musculature [HP:0003011] <3>(62|74) (69|31|7)
+ + 2:   Abnormality of muscle size [HP:0030236] <3>(6|6) (6|3|0)
+ + 2:   Abnormality of limbs [HP:0040064] <8>(57|64) (59|32|25)
+ + 2:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|34) (32|13|3)
+ 1:   Skeletal muscle atrophy [HP:0003202] <12>(3|3) (3|2|0)
+ 1:   Abnormality of the musculature of the limbs [HP:0009127] <10>(12|8) (14|4|2)
0:   Limb-girdle muscle atrophy [HP:0003797] <3>(1|0) (1|0|0)
- 1:   Limb-girdle muscular dystrophy [HP:0006785](0|0) (0|0|0)
- 1:   Pelvic girdle amyotrophy [HP:0008946](0|0) (0|0|0)
- 1:   Shoulder girdle muscle atrophy [HP:0003724](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
Actin-like ATPase domain0.00006769Direct


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)
Actin-like ATPase domain0.00003196Direct


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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