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Phenotypic Abnormality (PA): Hepatic fibrosis

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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)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of the digestive system [HP:0025031] <6>(67|77) (77|47|25)
+ + + 3:   Abnormality of the abdominal organs [HP:0002012] <6>(27|27) (30|14|4)
+ + 2:   Abnormality of the liver [HP:0001392] <4>(17|12) (17|7|0)
+ 1:   Abnormal liver morphology [HP:0410042] <25>(13|9) (13|4|0)
0:   Hepatic fibrosis [HP:0001395] <3>(2|0) (3|1|0)
- 1:   Congenital hepatic fibrosis [HP:0002612](0|0) (0|0|0)
- 1:   Hepatic bridging fibrosis [HP:0012852](0|0) (0|0|0)
- 1:   Periportal fibrosis [HP:0001405](0|0) (0|0|0)


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Superfamily

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SCOP termFDR (all)Annotation (direct or inherited)
GroEL equatorial domain-like0.00004125Direct
WD40 repeat-like0.00008071Direct


Plot distribution on phylogenetic tree for Superfamily and/or Family domains annotated by this phenotype term
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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)
GroEL equatorial domain-like0.00001832Direct
WD40 repeat-like0.00003684Direct
TPR-like0.0006871Direct

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Supra-domain (Duplex) in N- to C-terminal order FDR (all) Annotation (direct or inherited)
50978,50978
  • 50978 - WD40 repeat-like
  • 50978 - WD40 repeat-like
  • 0.0003451Direct


    Plot distribution on phylogenetic tree for Supra-domains (Single/Individual) annotated by this phenotype term
    Plot tree as:   Download Newick format tree:
    (show help)