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
03723 HMN5B neuropathy, motor, distal, hereditary, type Vb (HMN-5B) 614751 AD - - REEP1 - -
02921 SPG31 paraplegia, spastic, autosomal dominant, type 31 (SPG-31) 610250 AD 257 254 REEP1 - -
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