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Disease Ontology (DO): porphyria cutanea tarda

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

Root: DO Hierarchy (disease ontology from University of Maryland)

Shortest distance to current term (+ for parents, - for children) DO term [DO ID] <#Children> (#SF|#FA) #Supra-domain
(Single|Duplex|Triple)
+ + + + + 5:   disease [DOID:4] <8>
+ + + + 4:   disease of anatomical entity [DOID:7] <12>(143|187) (147|103|58)
+ + + + 4:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ + + 3:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
+ + + 3:   integumentary system disease [DOID:16] <3>(30|34) (31|15|6)
+ + 2:   porphyria [DOID:13268] <2>(0|0) (0|0|0)
+ + 2:   skin disease [DOID:37] <49>(27|31) (28|14|6)
+ 1:   acute porphyria [DOID:3133] <6>(0|0) (0|0|0)
+ 1:   dermatitis [DOID:2723] <18>(13|17) (14|6|4)
0:   porphyria cutanea tarda [DOID:3132](0|0) (0|0|0)