Phenotypes for disease #04543 (JLNS1 (Jervell and Lange-Nielsen syndrome (JLNS-1)), OMIM:220400)

16 entries on 1 page. Showing entries 1 - 16.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060504 Jervell and Lange-Nielsen syndrome (OMIM:220400) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080935
0000060646 Jervell and Lange-Nielsen syndrome (OMIM:220400) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00081077
0000119899 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147214
0000119923 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147238
0000119960 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147275
0000120016 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147331
0000120017 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147332
0000120061 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147376
0000120191 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147506
0000120238 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147553
0000120239 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147554
0000120248 Jervell and Lange-Nielsen Syndrome - - Familial, autosomal recessive - - - - - Johan den Dunnen 00147563
0000120292 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147607
0000120300 Jervell and Lange-Nielsen Syndrome - - Unknown - - - - - Johan den Dunnen 00147615
0000130091 - - - Familial, autosomal recessive - - - - - Samaneh Vojdani 00165219
0000130111 hearing loss, long QT - - Familial, autosomal recessive 05y 01y 00y06m 0m - Samaneh Vojdani 00165231
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