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Phenotypic Abnormality (PA): Erythema

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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:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + 4:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + + 4:   Phenotypic abnormality [HP:0000118] <25>
+ + + 3:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + + 3:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + 2:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + 2:   Generalized abnormality of skin [HP:0011354] <12>(8|12) (12|4|1)
+ 1:   Vascular skin abnormality [HP:0011276] <10>(6|10) (9|2|1)
0:   Erythema [HP:0010783] <7>(0|1) (1|0|0)
- 1:   Erythema migrans [HP:0031180](0|0) (0|0|0)
- 1:   Erythema of the eyelids [HP:0040323](0|0) (0|0|0)
- 1:   Facial erythema [HP:0001041](0|0) (0|0|0)
- 1:   Necrolytic migratory erythema [HP:0031181](0|0) (0|0|0)
- 1:   Palmoplantar erythema [HP:0025493](0|0) (0|0|0)
- 1:   Shawl sign [HP:0025535](0|0) (0|0|0)
- 1:   V-sign [HP:0025536](0|0) (0|0|0)


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

Family

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SCOP termFDR (all)Annotation (direct or inherited)
Intermediate filament protein, coiled coil region0.0005647Direct


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)
Intermediate filament protein, coiled coil region0.0005739Direct


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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