myotonia congenita

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muscle tissue disease that is characterised by slow muscle relaxation associated with hyperexcitation of the muscle fibres

Adnoddau allanol

dynodwr Freebase	/m/0820gw^[1]
dynodwr Microsoft Academic	2776767690 2909425333
dynodwr Quora	Myotonia-Congenita^[2]
PatientsLikeMe condition ID	myotonia-congenita
DiseasesDB	8736
Gran Enciclopèdia Catalana ID	miotonia-congenita
Orphanet ID	614^[3] 206973^[4] mapping relation type: exact match
Disease Ontology ID	DOID:2106^[5]
dynodwr Gran Enciclopèdia Catalana	0194512
WikiProjectMed ID	Myotonia congenita
Genetics Home Reference Conditions ID	myotonia-congenita
MedlinePlus ID	001424
Mondo ID	MONDO_0016121
dynodwr JSTOR (pwnc)	myotonia-congenita
ICD-10	G71.1
ICD-11 ID (MMS)	8C71.2 enwyd fel: Myotonia congenita
UMLS CUI	C0027127^[3]
dynodwr Encyclopædia Britannica Online	science/myotonia-congenita enwyd fel: myotonia congenita
GARD rare disease ID	12301^[3]
Cod MeSH	C05.651.662.500 C10.574.500.545 C10.668.491.606.500 C16.320.400.540
ICD-11 (foundation)	1916703439
ICD-10-CM	G71.1^[4]
dynodwr OMIM	160800^[3] 255700^[3]
dynodwr MeSH	D009224^[3] enwyd fel: Myotonia Congenita
dynodwr KEGG	H00705
OpenAlex ID	C2776767690^[6]

clefyd prin

dosbarth o glefyd

muscle tissue disease^[5]

channelopathy

Asmus Julius Thomsen

niwroleg

myotonia

ranolazine^[7]

CLCN1^[8]^[9]

359.22^[3]

C84912^[3]

Myotonia congenita

↑ Freebase Data Dumps, 28 Hydref 2013
↑ Quora
↑ ^3.0 ^3.1 ^3.2 ^3.3 ^3.4 ^3.5 ^3.6 ^3.7 Disease Ontology, 15 Mai 2019, DOID:2106
↑ ^4.0 ^4.1 Monarch Disease Ontology release 2018-06-29, 28 Gorffennaf 2018, MONDO_0016121
↑ ^5.0 ^5.1 ^5.2 Disease Ontology, 29 Tachwedd 2020, DOID:2106
↑ OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
↑ CHEMBL1404, 25 Mai 2016, ChEMBL, Saesneg
↑ 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