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
05223 CMS20 myasthenic syndrome, congenital, type 20, presynaptic (CMS-20) 617143 AR 6 6 SLC5A7 - -
01446 HMN7A neuropathy, motor, distal, hereditary, type VIIA (HMN-7A) 158580 AD - - SLC5A7 - -
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