All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02808 SNAX1 ataxia, sensory, type 1, autosomal dominant (SNAX-1) 608984 AD - - RNF170 - -
00325 SPG paraplegia, spastic (SPG) - - 127 121 AMFR, CAPN1, DDHD2, HPDL, RNF170, SPAST, SPG11, TECPR2, TMEM63C - -
07001 SPG85 paraplegia, spastic, autosomal recessive, type 85 619686 AR - - RNF170 - -
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