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3 OMIM references -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
7 signs/symptoms
Sarcoidosis
Graham Little-Piccardi-Lassueur syndrome

BTNL2 HLA-DRA
HLA-DRB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
HLA-DRB1
(0.88)
HLA-DRA



Citations in the biomedical literature:


Sarcoidosis
BTNL2 HLA-DRB1
Graham Little-Piccardi-Lassueur syndrome
HLA-DRA



Sarcoidosis
Graham Little-Piccardi-Lassueur syndrome

Synonym(s):
- Besnier-Boeck-Schaumann disease
- Boeck sarcoid
- Boeck's sarcoid

Synonym(s):
- Graham Little syndrome
- Piccardi-Lassueur-Little syndrome

Classification (Orphanet):
- Rare cardiac disease
- Rare endocrine disease
- Rare eye disease
- Rare neurologic disease
- Rare renal disease
- Rare respiratory disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease

Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the skin and subcutaneous tissue -

Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
(no data available)

External references:
3 OMIM references -
1 MeSH reference: D012507
External references:
No OMIM references
No MeSH references

Graham Little-Piccardi-Lassueur syndrome

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



Sarcoidosis

(no data available)