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Phenotypic Abnormality (PA): Atrophodermia vermiculata

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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:   Phenotypic abnormality [HP:0000118] <25>
+ + + + 4:   Abnormality of head or neck [HP:0000152] <2>(86|104) (97|58|38)
+ + + + 4:   Abnormality of the skin [HP:0000951] <4>(34|55) (45|36|12)
+ + + 3:   Abnormality of skin morphology [HP:0011121] <22>(29|49) (40|31|11)
+ + + 3:   Abnormality of the head [HP:0000234] <6>(85|102) (96|57|38)
+ + + 3:   Abnormality of connective tissue [HP:0003549] <12>(19|27) (19|20|20)
+ + 2:   Abnormality of the face [HP:0000271] <14>(70|85) (82|46|31)
+ + 2:   Localized skin lesion [HP:0011355] <29>(12|20) (18|10|6)
+ + 2:   Scarring [HP:0100699] <4>(1|2) (1|1|2)
+ 1:   Atypical scarring of skin [HP:0000987] <4>(1|2) (1|1|1)
+ 1:   Abnormality of facial soft tissue [HP:0011799] <7>(2|3) (4|3|0)
0:   Atrophodermia vermiculata [HP:0100837](0|0) (0|0|0)