myotonia congenita
(Q587420)
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
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Current Data About
myotonia congenita
| (P31) |
(Q929833)
(Q112193867) |
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| (P138) |
(Q6208773)
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| (P279) |
(Q18557307)
(Q2936142) |
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| (P373) |
Myotonia congenita
|
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| (P780) |
(Q1277793)
|
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| (P1692) |
359.22
|
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| (P1748) |
C84912
|
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| (P1995) |
(Q83042)
|
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| (P2176) |
(Q907104)
|
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| (P2293) |
(Q17862020)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_2106
http://identifiers.org/doid/DOID:2106
http://www.orpha.net/ORDO/Orphanet_206973 http://www.orpha.net/ORDO/Orphanet_614 |
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| (P5008) |
(Q4099686)
|
other details
| aliases |
Congenital myotonia, NOS Congenital myotonia, autosomal dominant form (disorder) Thomsen's disease Thomsen disease Congenital myotonia, autosomal dominant form |
| description | muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres |
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