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Phenotypic Abnormality (PA): Generalized neonatal 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)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ + + + 4:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
+ + + 3:   Abnormal muscle tone [HP:0003808] <3>(23|37) (27|15|5)
+ + 2:   Muscular hypotonia [HP:0001252] <9>(15|27) (18|9|4)
+ 1:   Neonatal hypotonia [HP:0001319] <1>(0|0) (1|1|0)
0:   Generalized neonatal hypotonia [HP:0008935](0|0) (1|0|0)


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)
RING/U-box0.0006488Direct


Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
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