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
00451 Gaucher, atypical Gaucher disease, atypical 610539 - 1 1 PSAP - -
00450 Krabbe, atypical Krabbe disease, atypical 611722 AR - - PSAP - -
00449 MLDB leukodystrophy, metachromatic, due to saposin-B deficiency 249900 AR 32 31 PSAP - -
00452 PSAPD saposin deficiency, combined (PSAPD) 611721 AR 3 3 PSAP - -
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