oculogastrointestinal muscular dystrophy https://github.com/monarch-initiative/mondo/issues/6745 https://www.malacards.org/card/visceral_myopathy_familial_with_external_ophthalmoplegia SCTID:722060007 Orphanet:1876 visceral myopathy - familial external ophthalmoplegia GARD:0005496 MEDGEN:336376 Oculogastrointestinal muscular dystrophy is an extremely rare autosomal recessively inherited neuromuscular disease characterized by ocular manifestations such as ptosis and diplopia followed by chronic diarrhea, malnutrion and intestinal peudo-obstruction. UMLS:C1848586 OMIM:277320 familial visceral myopathy with external ophthalmoplegia MONDO:0010181 icd11.foundation:1205053137 visceral myopathy-familial external ophthalmoplegia syndrome intestinal motility disease disorder of visual system