Monarch Disease Ontology id MONDO_0010181 (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. Also known as: visceral myopathy-familial external ophthalmoplegia syndrome.