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
00325 SPG paraplegia, spastic (SPG) - - 165 158 AMFR, CAPN1, DDHD2, HPDL, RNF170, SPAST, SPG11, TECPR2, TMEM63C - -
07085 SPG89 paraplegia, spastic, type 89, autosomal recessive 620379 AR - - AMFR - -
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