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Phenotypic Abnormality (PA): Myotonia

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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)
+ + + 3:   Phenotypic abnormality [HP:0000118] <25>
+ + 2:   Abnormality of the musculature [HP:0003011] <3>(64|83) (70|33|9)
+ 1:   Abnormal muscle physiology [HP:0011804] <12>(44|59) (51|22|5)
0:   Myotonia [HP:0002486] <10>(0|0) (0|0|0)
- 1:   Percussion myotonia [HP:0010548] <2>(0|0) (0|0|0)
- 1:   Cold-sensitive myotonia [HP:0012904](0|0) (0|0|0)
- 1:   EMG: myotonic runs [HP:0003730](0|0) (0|0|0)
- 1:   Handgrip myotonia [HP:0012899](0|0) (0|0|0)
- 1:   Myotonia of the face [HP:0012900](0|0) (0|0|0)
- 1:   Myotonia of the jaw [HP:0012901](0|0) (0|0|0)
- 1:   Myotonia of the lower limb [HP:0012902](0|0) (0|0|0)
- 1:   Myotonia of the upper limb [HP:0012903](0|0) (0|0|0)
- 1:   Myotonia with warm-up phenomenon [HP:0003740](0|0) (0|0|0)
- 1:   Paradoxical myotonia [HP:0011809](0|0) (0|0|0)