Narcolepsy 3

MONDO:0012179

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.

Also known as: NRCLP3, narcolepsy 3

20 clinical trials for this condition and its sub-types.

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