All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00499 SMA-1 atrophy, muscular, spinal, type 1 (Werdnig-Hoffman disease, severe infantile acute) 253300 - - - SMN1 - -
00500 SMA-2 atrophy, muscular, spinal, type II (infantile, chronic) 253550 - - - SMN1 - -
00501 SMA-3 atrophy, muscular, spinal, type III (juvenile, Wohlfart-Kugelberg-Welander disease) 253400 - - - SMN1, SMN2 - -
00502 SMA-4 atrophy, muscular, spinal, type IV (adult) 271150 - - - SMN1 - -
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