All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01783 FRBRL Farber lipogranulomatosis (FRBRL) 228000 - 1 1 ASAH1 - -
01452 SMAPME atrophy, muscular, spinal, with progressive myoclonic epilepsy (SMAPME) 159950 - 7 7 ASAH1 - -
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