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) - - 127 121 AMFR, CAPN1, DDHD2, HPDL, RNF170, SPAST, SPG11, TECPR2, TMEM63C - -
01560 SPG4 paraplegia, spastic, autosomal dominant, type 4 (SPG4) 182601 AD 12 12 SPAST - -
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