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Up to: Hereditary neurological disease · Narcolepsy-cataplexy syndrome · Hereditary narcolepsy
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.
This condition has no sub-types.