Preferred Name

MYOTONIA CONGENITA, AUTOSOMAL DOMINANT

Synonyms

MYOTONIA LEVIOR

ID

http://purl.bioontology.org/ontology/OMIM/160800

altLabel

MYOTONIA LEVIOR

THOMSEN DISEASE

THD

cui

C0270959

C2936781

Gene Locus

7q35

Gene Symbol

CLCN1

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU004173

http://purl.bioontology.org/ontology/OMIM/MTHU016903

http://purl.bioontology.org/ontology/OMIM/MTHU010827

http://purl.bioontology.org/ontology/OMIM/MTHU010825

http://purl.bioontology.org/ontology/OMIM/MTHU025982

http://purl.bioontology.org/ontology/OMIM/MTHU025980

http://purl.bioontology.org/ontology/OMIM/MTHU010830

http://purl.bioontology.org/ontology/OMIM/MTHU005259

http://purl.bioontology.org/ontology/OMIM/MTHU016378

http://purl.bioontology.org/ontology/OMIM/MTHU010824

http://purl.bioontology.org/ontology/OMIM/MTHU026511

http://purl.bioontology.org/ontology/OMIM/MTHU025981

http://purl.bioontology.org/ontology/OMIM/MTHU010823

http://purl.bioontology.org/ontology/OMIM/MTHU010826

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

160800

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

MYOTONIA CONGENITA, AUTOSOMAL DOMINANT

Scope Statement

Highly variable phenotype and severity [MISCELLANEOUS]

Warm weather and alcohol are alleviating factors [MISCELLANEOUS]

Affected females report aggravation of symptoms during menstrual periods and pregnancy, with alleviation after menopause [MISCELLANEOUS]

Caused by mutation in the skeletal muscle chloride channel-1 gene (CLCN1, 118425.0002) [MOLECULAR BASIS]

Onset in childhood, adolescence [MISCELLANEOUS]

Cold temperatures exacerbate symptoms [MISCELLANEOUS]

See also autosomal recessive form (255700), which is more common and more severe [MISCELLANEOUS]

Worldwide prevalence of 1/100,000 [MISCELLANEOUS]

Increased prevalence in Northern Finland (7.3/100,000) [MISCELLANEOUS]

tui

T047

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/D009224 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/MESH/D009224 Medical Subject Headings / 医学主题词表 CUI
http://purl.obolibrary.org/obo/MONDO_0008055 Mondo Disease Ontology / Mondo疾病本体 LOOM
http://purl.bioontology.org/ontology/ICD10CM/G71.12 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI
http://purl.bioontology.org/ontology/ICD10CM/G71.12 International Classification of Diseases, Version 10 - Clinical Modification / 国际疾病分类,第10版-临床修改 CUI