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
04249 macular dystrophy dystrophy, macular - - 896 568 AP5B1, AP5M1, AP5Z1, SAMD7 - -
03377 SPG48 paraplegia, spastic, type 48, autosomal recessive 613647 AR - - AP5Z1 - -
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