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
03101 HLD4 leukodystrophy, hypomyelinating, type 4 (HLD-4) 612233 AR - - HSPD1 - -
02538 SPG13 paraplegia, spastic, type 13 (SPG-13) 605280 AD - - HSPD1 - -
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