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
03888 SMALED2A atrophy, muscular, spinal, lower extremity predominant, type 2A 615290 AD 2 2 BICD2 - autosomal dominant inheritance
06825 SMALED2B spinal muscular atrophy, lower extremity-predominant, type 2B 618291 AD - - BICD2 - -
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