has material basis in germline mutation in STIM1 Stormorken syndrome https://www.malacards.org/card/stormorken_syndrome 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. SCTID:711407000 Stormorken syndrome Orphanet:3204 OMIM:185070 MESH:C566108 ICD9:759.89 MEDGEN:350028 DOID:0060354 Thrombocytopathy-asplenia-miosis syndrome MONDO:0008497 STRMK GARD:0005188 UMLS:C1861451 Thrombocytopathy asplenia miosis syndromic constitutional thrombocytopenia