SUPERFAMILY 1.75 HMM library and genome assignments server

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Phenotypic Abnormality (PA): Dementia

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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 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:   Abnormality of higher mental function [HP:0011446] <9>(38|45) (40|24|8)
+ + 2:   Cognitive impairment [HP:0100543] <3>(4|5) (6|4|0)
+ 1:   Mental deterioration [HP:0001268] <5>(0|1) (1|1|0)
0:   Dementia [HP:0000726] <4>(0|0) (1|0|0)
- 1:   Frontotemporal dementia [HP:0002145] <1>(0|0) (1|0|0)
- 1:   Frontal lobe dementia [HP:0000727](0|0) (0|0|0)
- 1:   Frontolimbic dementia [HP:0002439](0|0) (0|0|0)
- 1:   Subcortical dementia [HP:0007123](0|0) (0|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)
RNA-binding domain, RBD0.1879Inherited


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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