Cytoscape Web
Click node...

Narcolepsy without cataplexy
3 associated genes
20 connected diseases
4 signs/symptoms
Disease Type of connection
Bullous pemphigoid
Diffuse cutaneous systemic sclerosis
Follicular lymphoma
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
Graham Little-Piccardi-Lassueur syndrome
17p13.3 microduplication syndrome
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Behavioral variant of frontotemporal dementia
Common variable immunodeficiency
Distal 17p13.3 microdeletion syndrome
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Miller-Dieker syndrome
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Precursor T-cell acute lymphoblastic leukemia
(no synonyms)

Classification (Orphanet):
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adolescence / young
Average age of death: normal
Type of inheritance: unknown
External references:
No OMIM references
No MeSH references

Gene symbol UniProt reference OMIM reference
HCRT O43612602358
HLA-DQB1 P01920604305
HLA-DRB1 P04229142857
Very frequent
- Delirium / hallucination
- Sleep and vigilance disorders
- Somnolence / hypersomnia / parasomnia

- Psychic / behavioural troubles