SUPERFAMILY 1.75 HMM library and genome assignments server

Superfamily is undergoing a server migration - you are now browsing on the new server. Please contact us if you experience any problems.

Phenotypic Abnormality (PA): Rhabdomyolysis

(show info)

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

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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormal skeletal muscle morphology [HP:0011805] <38>(30|36) (35|14|4)
0:   Rhabdomyolysis [HP:0003201] <5>(0|0) (0|0|0)
- 1:   Acute rhabdomyolysis [HP:0008942](0|0) (0|0|0)
- 1:   Alcohol-induced rhabdomyolysis [HP:0011440](0|0) (0|0|0)
- 1:   Anesthetic-induced rhabdomylosis [HP:0011439](0|0) (0|0|0)
- 1:   Exercise-induced rhabdomyolysis [HP:0009045](0|0) (0|0|0)
- 1:   Viral infection-induced rhabdomyolysis [HP:0003558](0|0) (0|0|0)