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
04090 PCH9 hypoplasia, pontocerebellar, type 9 (PCH-9) 615809 AR 15 16 AMPD2 - -
04049 SPG63 paraplegia, spastic, type 63, autosomal recessive (SPG-63) 615686 AR - - AMPD2 - -
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