myotonia congenita
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
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myotonia congenita
Summary
myotonia congenita is a rare disease[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- myotonia congenita's instance of is recorded as rare disease[3].
- myotonia congenita's instance of is recorded as class of disease[4].
- Asmus Julius Thomsen is named after myotonia congenita[5].
- myotonia congenita is a type of muscle tissue disease[6].
- myotonia congenita is a type of channelopathy[7].
- myotonia congenita's Commons category is recorded as Myotonia congenita[8].
- myotonia congenita's symptoms and signs is recorded as myotonia[9].
- myotonia congenita's ICD-9-CM is recorded as 359.22[10].
- myotonia congenita's NCI Thesaurus ID is recorded as C84912[11].
- myotonia congenita's health specialty is recorded as neurology[12].
- myotonia congenita's drug or therapy used for treatment is recorded as ranolazine[13].
- myotonia congenita's genetic association is recorded as CLCN1[14].
- myotonia congenita's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2106[15].
- myotonia congenita's exact match is recorded as http://identifiers.org/doid/DOID:2106[16].
- myotonia congenita's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_206973[17].
- myotonia congenita's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_614[18].
- myotonia congenita's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
myotonia congenita has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[20]