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Graham Little-Piccardi-Lassueur syndrome
1 associated gene
12 connected diseases
7 signs/symptoms
Disease Type of connection
Bullous pemphigoid
Diffuse cutaneous systemic sclerosis
Follicular lymphoma
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
Narcolepsy without cataplexy
Narcolepsy-cataplexy
Sarcoidosis
Common variable immunodeficiency
17p13.3 microduplication syndrome
Distal 17p13.3 microdeletion syndrome
Miller-Dieker syndrome
Synonym(s):
- Graham Little syndrome
- Piccardi-Lassueur-Little syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
HLA-DRA P01903142860
Very frequent
- Alopecia
- Decreased body hair / axillar / pubic hairlessness
- Follicular / erythematous / edematous papules / milium
- Hyperkeratosis / ainhum / hyperkeratotic skin fissures
- Hypotrichosis / atrichia / atrichiasis / scalp hairlessness

Frequent
- Lichen
- Pruritus / itching