disorder of glycogen metabolism movement disorder Lafora disease https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://rarediseases.info.nih.gov/diseases/8214/lafora-disease https://www.malacards.org/card/myoclonic_epilepsy_of_lafora_1 MEDGEN:155631 NANDO:1200955 NORD:143373 Lafora body disease progressive myoclonic epilepsy type 2 Lafora body disorder epilepsy, progressive myoclonic, 2A epilepsy, progressive myoclonic, 2B DOID:3534 Melf Orphanet:501 Lafora disease EPM2 PME type 2 epilepsy, progressive myoclonic 2A (Lafora) MESH:D020192 OMIMPS:254780 MONDO:0009697 Lafora disease (LD) is a rare, inherited, severe, progressive myoclonic epilepsy characterized by myoclonus and/or generalized seizures, visual hallucinations (partial occipital seizures), and progressive neurological decline. NANDO:2200881 Epm2 MedDRA:10054030 progressive myoclonus epilepsy type 2 NCIT:C84804 SCTID:230425004 GARD:0008214 myoclonic epilepsy of Lafora epilepsy, progressive myoclonic 2B (Lafora) epilepsy progressive myoclonic 2 UMLS:C0751783 progressive myoclonus epilepsy