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Phenotypic Abnormality (PA): Increased cerebral lipofuscin

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the nervous system [HP:0000707] <4>(142|168) (156|103|45)
+ + + 3:   Abnormality of nervous system morphology [HP:0012639] <5>(69|97) (79|52|16)
+ + 2:   Morphological abnormality of the central nervous system [HP:0002011] <17>(60|85) (69|44|16)
+ 1:   Atrophy/Degeneration affecting the central nervous system [HP:0007367] <10>(3|5) (5|3|0)
0:   Increased cerebral lipofuscin [HP:0011813] <2>(0|0) (0|0|0)
- 1:   Increased extraneuronal autofluorescent lipopigment [HP:0003463](0|0) (0|0|0)
- 1:   Increased neuronal autofluorescent lipopigment [HP:0002074](0|0) (0|0|0)