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
01744 RTSC1 Ritscher-Schinzel syndrome 1 220210 AR - - KIAA0196 - -
00217 SPG8 paraplegia, spastic, autosomal dominant, type 8 (SPG-8) 603563 AD 2 2 KIAA0196 - -
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