All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00044 FAF amyloidosis, Finnish type (type V) (FAF) 105120 - 24 24 GSN - -
01935 MPS-3C mucopolysaccharidosis, type IIIC (MPS-3C) 252930 - 110 110 HGSNAT - -
04500 RP73 retinitis pigmentosa, type 73 (RP73) 616544 - 0 0 HGSNAT - -
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