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
07238 HMNR10 neuronopathy, distal hereditary motor, autosomal recessive, type 10 620542 AR - - VRK1 - -
02676 PCH1A hypoplasia, pontocerebellar, type 1A 607596 AR 1 1 VRK1 - -
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