MeSH Browser

MeSH Heading: Jervell-Lange Nielsen Syndrome
Tree Number(s): C14.280.067.565.440; C14.280.123.625.440; C16.131.240.400.715.440
Unique ID: D029593
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D029593
Scope Note: 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).
Entry Term(s): Cardio-Auditory-Syncope Syndrome; Cardioauditory Syndrome of Jervell and Lange-Nielsen; Deafness, Congenital, and Functional Heart Disease; Jervell And Lange-Nielsen Syndrome 1; Jervell and Lange-Nielsen Syndrome; Prolonged QT Interval in EKG and Sudden Death; Surdo-Cardiac Syndrome
Previous Indexing: Deafness (1969-1985); Long QT Syndrome (1986-2001)
See Also: KCNQ1 Potassium Channel
Public MeSH Note: 2002; see LONG QT SYNDROME 1986-2001
History Note: 2002; use LONG QT SYNDROME 1986-2001
Date Established: 2002/01/01
Date of Entry: 2001/07/25
Revision Date: 2019/07/05

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Jervell-Lange Nielsen Syndrome MeSH Descriptor Data 2023