MONDO_0008497 (Stormorken syndrome) can be described as follows. Stormorken-Sjaastad-Langslet syndrome is characterized by thrombocytopathy, asplenia, miosis, muscle fatigue, migraine, dyslexia, and ichthyosis. It has been described in six members of one family. It is transmitted as an autosomal dominant trait. Also known as: Thrombocytopathy-asplenia-miosis syndrome, thrombocytopathy, asplenia and miosis.