Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
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.
Features include always present findings: Abnormal rapid eye movement sleep. 5 total HPO annotations.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Brain and nerves | 2 | Hypnagogic hallucination, Excessive daytime somnolence |
Eyes |
Biomarker and diagnostic research for narcolepsy 3 has been reported in the published literature.
Phenotype severity distribution: 1 always present feature.
No clinical trials have been registered for narcolepsy 3.
202 publications have been identified in PubMed for narcolepsy 3. Kisho has analyzed 94 by research type. Research spans Epidemiology / Natural History (32%), Basic Science / Preclinical (18%), and Review / Meta-Analysis (16%).
Research Type | Count | % of Total |
|---|---|---|
Disease patterns and progression | 30 | 32% |
Data assembled from 4 of 12 sources · Last updated Sep 19, 2026, 12:36 PM UTC
Program availability and eligibility requirements are set by each foundation. Contact them directly to learn more about your options.
Claim this page and your organization will be listed here for patients and families to find.
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
1
Abnormal rapid eye movement sleep |
Laboratory research
17 |
18% |
Research summaries | 15 | 16% |
Clinical study results | 15 | 16% |
Testing and diagnosis research | 7 | 7% |
Other research | 6 | 6% |
Patient case studies | 3 | 3% |
New treatment approaches | 1 | 1% |
Sabnis RW (2026). [PMID: 42157843](https://pubmed.ncbi.nlm.nih.gov/42157843/). *ACS Med Chem Lett*. [Other]
Honda M (2026). [PMID: 41551896](https://pubmed.ncbi.nlm.nih.gov/41551896/). *Sleep Biol Rhythms*. [Other]
Karas M (2026). [PMID: 41342419](https://pubmed.ncbi.nlm.nih.gov/41342419/). *Sleep*. [Diagnostic / Biomarker]
Jennum PJ (2026). [PMID: 41520546](https://pubmed.ncbi.nlm.nih.gov/41520546/). *Sleep Med*. [Epidemiology / Natural History]
Mullen JM (2026). [PMID: 29493990](https://pubmed.ncbi.nlm.nih.gov/29493990/). *Unknown Journal*. [Epidemiology / Natural History]
Deventer MH (2026). [PMID: 41581719](https://pubmed.ncbi.nlm.nih.gov/41581719/). *Eur J Pharmacol*. [Basic Science / Preclinical]
Adenan MH (2026). [PMID: 41526185](https://pubmed.ncbi.nlm.nih.gov/41526185/). *Pract Neurol*. [Review / Meta-Analysis]
Arif Z (2026). [PMID: 41497057](https://pubmed.ncbi.nlm.nih.gov/41497057/). *Ann Med Surg (Lond)*. [Other]
Woodliff B (2026). [PMID: 42044244](https://pubmed.ncbi.nlm.nih.gov/42044244/). *Unknown Journal*. [Epidemiology / Natural History]
Bassetti CLA (2026). [PMID: 41689412](https://pubmed.ncbi.nlm.nih.gov/41689412/). *Eur J Neurol*. [Review / Meta-Analysis]