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Phenotypic Abnormality (PA): Erythema of the eyelids

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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)
+ + + + + + + 7:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + + + 6:   Abnormality of the integument [HP:0001574] <4>(48|69) (59|37|15)
+ + + + + + 6:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + + + 5:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + + + 5:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + + + 4:   Abnormality of the orbital region [HP:0000315] <4>(17|24) (19|5|4)
+ + + + 4:   Abnormality of the cardiovascular system [HP:0001626] <5>(60|88) (73|43|30)
+ + + + 4:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + + 3:   Abnormality of the ocular adnexa [HP:0032039] <2>(17|24) (19|5|4)
+ + + 3:   Generalized abnormality of skin [HP:0011354] <12>(8|12) (12|4|1)
+ + + 3:   Abnormality of the vasculature [HP:0002597] <13>(35|56) (45|27|18)
+ + 2:   Vascular skin abnormality [HP:0011276] <10>(6|10) (9|2|1)
+ + 2:   Abnormal ocular adnexa morphology [HP:0030669] <6>(17|24) (19|5|4)
+ 1:   Erythema [HP:0010783] <7>(0|1) (1|0|0)
+ 1:   Abnormal eyelid morphology [HP:0000492] <26>(10|17) (12|2|3)
0:   Erythema of the eyelids [HP:0040323](0|0) (0|0|0)