myotonia congenita

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

External resources

Freebase ಐಡಿ
Microsoft Academic ID
Quora topic ID
PatientsLikeMe condition ID
DiseasesDB
Gran Enciclopèdia Catalana ID
Orphanet ID
206973[]

mapping relation type: exact match

Disease Ontology ID
Gran Enciclopèdia Catalana ID (former scheme)
WikiProjectMed ID
Genetics Home Reference Conditions ID
MedlinePlus ID
Mondo ID
JSTOR topic ID (archived)
ICD-10 ID
ICD-11 ID (MMS)
8C71.2

subject named as: Myotonia congenita

UMLS CUI
Encyclopædia Britannica Online ID
science/myotonia-congenita

subject named as: myotonia congenita

GARD rare disease ID
MeSH tree code
ICD-11 ID (Foundation)
ICD-10-CM
OMIM ID
MeSH descriptor ID
D009224[]

subject named as: Myotonia Congenita

KEGG ID
OpenAlex ID

ಉದಾಹರಣೆಗೆ

rare disease
class of disease

ಉಪವರ್ಗ

muscle tissue disease[]
channelopathy

ಸ್ಮರಣಾರ್ಥ

Asmus Julius Thomsen

symptoms and signs

myotonia

drug or therapy used for treatment

ranolazine[]

genetic association

on focus list of Wikimedia project

WikiProject Medicine

ICD-9-CM

359.22[]

NCI Thesaurus ID

C84912[]

ಕಾಮನ್ಸ್ ವರ್ಗ

Myotonia congenita

Reference

  1. Freebase Data Dumps, ೨೮ ಅಕ್ಟೋಬರ್ 2013
  2. Quora
  3. ೩.೦ ೩.೧ ೩.೨ ೩.೩ ೩.೪ ೩.೫ ೩.೬ ೩.೭ Disease Ontology, ೧೫ ಮೇ 2019, DOID:2106
  4. ೪.೦ ೪.೧ Monarch Disease Ontology release 2018-06-29, ೨೮ ಜುಲೈ 2018, MONDO_0016121
  5. ೫.೦ ೫.೧ ೫.೨ Disease Ontology, ೨೯ ನವೆಂಬರ್ 2020, DOID:2106
  6. OpenAlex, ೨೬ ಜನವರಿ 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  7. CHEMBL1404, ೨೫ ಮೇ 2016, ಆಂಗ್ಲ, ChEMBL
  8. Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
  9. The skeletal muscle chloride channel in dominant and recessive human myotonia
  10. Identifiers.org, https://registry.identifiers.org/registry/doid
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