myotonia congenita
ಗೋಚರ
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
ಉದಾಹರಣೆಗೆ
rare disease
class of disease
ಸ್ಮರಣಾರ್ಥ
Asmus Julius Thomsen
health specialty
symptoms and signs
myotonia
drug or therapy used for treatment
ranolazine[೭]
on focus list of Wikimedia project
WikiProject Medicine
ICD-9-CM
359.22[೩]
NCI Thesaurus ID
C84912[೩]
exact match
ಕಾಮನ್ಸ್ ವರ್ಗ
Myotonia congenita
Reference
- ↑ Freebase Data Dumps, ೨೮ ಅಕ್ಟೋಬರ್ 2013
- ↑ Quora
- ↑ ೩.೦ ೩.೧ ೩.೨ ೩.೩ ೩.೪ ೩.೫ ೩.೬ ೩.೭ Disease Ontology, ೧೫ ಮೇ 2019, DOID:2106
- ↑ ೪.೦ ೪.೧ Monarch Disease Ontology release 2018-06-29, ೨೮ ಜುಲೈ 2018, MONDO_0016121
- ↑ ೫.೦ ೫.೧ ೫.೨ Disease Ontology, ೨೯ ನವೆಂಬರ್ 2020, DOID:2106
- ↑ OpenAlex, ೨೬ ಜನವರಿ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ CHEMBL1404, ೨೫ ಮೇ 2016, ಆಂಗ್ಲ, 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