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

28 clinical trials for this condition and its sub-types, 0 tagged with Narcolepsy 3 itself.

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↑ Hereditary neurological disease (5791) ↑ Narcolepsy-cataplexy syndrome (44) ↑ Hereditary narcolepsy (5)

Including sub-types (28) Tagged with Narcolepsy 3 (0)

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