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Phenotypic Abnormality (PA): Moderate global developmental delay

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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> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + + 4:   Abnormality of nervous system physiology [HP:0012638] <26>(101|119) (112|81|39)
+ + + 3:   Neurodevelopmental abnormality [HP:0012759] <5>(36|53) (39|26|12)
+ + 2:   Neurodevelopmental delay [HP:0012758] <4>(17|30) (18|10|2)
+ 1:   Global developmental delay [HP:0001263] <4>(10|17) (11|3|0)
0:   Moderate global developmental delay [HP:0011343](0|0) (0|0|0)