Disease #05223 (CMS20 (myasthenic syndrome, congenital, type 20, presynaptic (CMS-20)), OMIM:617143)

Official abbreviation CMS20
Name myasthenic syndrome, congenital, type 20, presynaptic (CMS-20)
OMIM ID 617143
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene SLC5A7
Associated tissues -
Disease features -
Remarks -
Date created 2017-02-10 16:34:12 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00100311 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents/sib M no France - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 2 1 Johan den Dunnen
00100312 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family, 1affected, unaffected heterozygous carrier parents M ? Algeria - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 1 1 Johan den Dunnen
00100313 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M - France - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 2 2 Johan den Dunnen
00100314 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F - Italy - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 2 1 Johan den Dunnen
00100315 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family,1 affected, unaffected heterozygous carrier parents M - Italy - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 2 1 Johan den Dunnen
00100316 - PubMed: Bauche 2016, Journal: Bauche 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Romania - - - - - CMS20 see paper; ... SLC5A7 SLC5A7 2 1 Johan den Dunnen
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