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Phenotypic Abnormality (PA): Absent speech

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

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 nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Neurodevelopmental abnormality [HP:0012759] <5>(36|53) (39|26|12)
+ + + 3:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + 2:   Abnormality of higher mental function [HP:0011446] <9>(38|45) (40|24|8)
+ + 2:   Neurodevelopmental delay [HP:0012758] <4>(17|30) (18|10|2)
+ 1:   Neurological speech impairment [HP:0002167] <20>(5|9) (5|4|1)
+ 1:   Delayed speech and language development [HP:0000750] <3>(1|4) (1|1|0)
0:   Absent speech [HP:0001344](0|1) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
L-arabinose binding protein-like0.0002459Direct


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