All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02638 meningioma meningioma, familial, susceptibility to 607174 - 64 64 MN1, NF2, PDGFB, PTEN, SMARCE1, SUFU - -
00499 SMA-1 atrophy, muscular, spinal, type 1 (SMA-1, Werdnig-Hoffman disease, severe infantile acute) 253300 - 30 30 SMN1 - -
00500 SMA-2 atrophy, muscular, spinal, type II (SMA-2, infantile, chronic) 253550 - 21 19 SMN1 - -
00501 SMA-3 atrophy, muscular, spinal, type III (SMA-3, juvenile, Wohlfart-Kugelberg-Welander disease) 253400 - 25 24 SMN1, SMN2 - -
00502 SMA-4 atrophy, muscular, spinal, type IV (SMA-4, adult) 271150 - 2 2 SMN1 - -
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