myotonia congenita
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
ઉદાહરણ
rare disease
class of disease
પરથી નામકરણ થયેલ
Asmus Julius Thomsen
health specialty
neurology
symptoms and signs
myotonia
drug or therapy used for treatment
ranolazine[૭]
on focus list of Wikimedia project
WikiProject Medicine
ICD-9-CM
359.22[૩]
NCI Thesaurus ID
C84912[૩]
exact match
કોમન્સ શ્રેણી
Myotonia congenita
સંદર્ભ
- ↑ Freebase Data Dumps, ૨૮ ઓક્ટોબર 2013
- ↑ ક્વોરા
- ↑ ૩.૦ ૩.૧ ૩.૨ ૩.૩ ૩.૪ ૩.૫ ૩.૬ ૩.૭ Disease Ontology, ૧૫ મે 2019, DOID:2106
- ↑ ૪.૦ ૪.૧ Monarch Disease Ontology release 2018-06-29, ૨૮ જુલાઇ 2018, MONDO_0016121
- ↑ ૫.૦ ૫.૧ ૫.૨ Disease Ontology, ૨૯ નવેમ્બર 2020, DOID:2106
- ↑ OpenAlex, ૨૬ જાન્યુઆરી 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ CHEMBL1404, ૨૫ મે 2016, અંગ્રેજી, ChEMBL
- ↑ Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
- ↑ The skeletal muscle chloride channel in dominant and recessive human myotonia
- ↑ Identifiers.org, https://registry.identifiers.org/registry/doid