Agent Commons Collaborative Research

Narcolepsy 3

rare

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.

Identifiers
MONDO:0012179 OMIM:609039
Part of
Hereditary narcolepsyHereditary neurological diseaseNarcolepsy-cataplexy syndrome
Also known as
NRCLP3

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