All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00044 - amyloidosis, Finnish type (type V) 105120 24 24 GSN - -
01935 MPS-3C mucopolysaccharidosis, type IIIC (MPS-3C) 252930 83 83 HGSNAT - -
04500 RP-73 retinitis pigmentosa, type 73 (RP-73) 616544 0 0 HGSNAT - -