SUPERFAMILY 1.75 HMM library and genome assignments server

SUPERFAMILY 2 can be accessed from supfam.org. Please contact us if you experience any problems.

Disease Ontology (DO): pseudo-Hurler polydystrophy

(show info)

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)
+ + + + 4:   disease [DOID:4] <8>
+ + + 3:   disease of metabolism [DOID:0014667] <2>(22|34) (27|12|5)
+ + 2:   inherited metabolic disorder [DOID:655] <18>(12|15) (16|5|0)
+ 1:   lysosomal storage disease [DOID:3211] <12>(6|5) (6|2|0)
0:   pseudo-Hurler polydystrophy [DOID:0080071](0|0) (0|0|0)