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
03400 HSN-1D neuropathy, sensory, hereditary, type ID (HSN-1D) 613708 - 0 0 ATL1 - -
00289 SPG-3A paraplegia, spastic, autosomal dominant, type 3A (SPG-3A) 182600 - 698 697 ATL1 - autosomal dominant
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