myotonia congenita
muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres
instancë e
rare disease
class of disease
emëruar prej
Asmus Julius Thomsen
health specialty
simptomat
myotonia
drug or therapy used for treatment
ranolazine[7]
on focus list of Wikimedia project
WikiProject Medicine
ICD-9-CM
359.22[3]
NCI Thesaurus ID
C84912[3]
përputhje e saktë
kategoria në Commons
Myotonia congenita
Reference
- ^ Freebase Data Dumps, 28 tetor 2013
- ^ Quora
- ^ a b c d e f g h Disease Ontology, 15 maj 2019, DOID:2106
- ^ a b Monarch Disease Ontology release 2018-06-29, 28 korrik 2018, MONDO_0016121
- ^ a b c Disease Ontology, 29 nëntor 2020, DOID:2106
- ^ OpenAlex, 26 janar 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ^ CHEMBL1404, 25 maj 2016, ChEMBL, anglisht
- ^ 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