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1 Possible Causes for Caused by Mutation in the Ceramide Synthase 1 Gene

  • Progressive Myoclonic Epilepsy Type 8

    Help Watch the 'search for a disease' video tutorial Procedures: Orphanet inventory of rare diseases Orphanet maintains the Orphanet nomenclature of rare diseases, essential in improving the visibility of rare diseases in health and research information systems: each disease in Orphanet is attributed a unique and[…][]

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