narcolepsy 3 https://github.com/monarch-initiative/mondo/issues/9082 https://www.malacards.org/card/narcolepsy_3 A rare, autosomal dominant form of narcolepsy mapped to chromosome 21q, between genetic markers D21S267 and ABCG1. 6 patients with the milder form were DQB1*0602-positive. narcolepsy 3 MEDGEN:332320 MONDO:0012179 NRCLP3 OMIM:609039 GARD:0015447 UMLS:C1836907 narcolepsy-cataplexy syndrome hereditary neurological disease hereditary narcolepsy