Jervell-Lange Nielsen Syndrome

"Jervell-Lange Nielsen Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

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A form of long QT syndrome that is associated with congenital deafness. It is characterized by abnormal cardioelectrophysiology involving the VOLTAGE-GATED POTASSIUM CHANNEL. It results from mutation of KCNQ1 gene (Subtype 1 or JLN1) or the KCNE1 gene (Subtype 2 or JLN2).

Descriptor ID

D029593

MeSH Number(s)

C14.280.067.565.440

C16.131.240.400.715.440

Concept/Terms

Jervell-Lange Nielsen Syndrome

Below are MeSH descriptors whose meaning is more general than "Jervell-Lange Nielsen Syndrome".

Diseases [C]
Cardiovascular Diseases [C14]
Heart Diseases [C14.280]
Arrhythmias, Cardiac [C14.280.067]
Long QT Syndrome [C14.280.067.565]
Jervell-Lange Nielsen Syndrome [C14.280.067.565.440]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Cardiovascular Abnormalities [C16.131.240]
Heart Defects, Congenital [C16.131.240.400]
Long QT Syndrome [C16.131.240.400.715]
Jervell-Lange Nielsen Syndrome [C16.131.240.400.715.440]

Below are MeSH descriptors whose meaning is related to "Jervell-Lange Nielsen Syndrome".

Below are MeSH descriptors whose meaning is more specific than "Jervell-Lange Nielsen Syndrome".

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This graph shows the total number of publications written about "Jervell-Lange Nielsen Syndrome" by people in Harvard Catalyst Profiles by year, and whether "Jervell-Lange Nielsen Syndrome" was a major or minor topic of these publication.

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J Med Case Rep
Heart Rhythm
Circ Arrhythm Electrophysiol
J Physiol