All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06195 CMS25 Myasthenic syndrome, congenital, 25 618323 AR 2 - VAMP1 - -
01186 SPAX1 ataxia, spastic, type 1, autosomal dominant (SPAX-1) 108600 AD 2 2 VAMP1 - -
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