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1 OMIM reference -
1 associated gene
18 signs/symptoms
PROTEIN INTERACTIONS: 1
3 OMIM references -
5 associated genes
No signs/symptoms info
Pyogenic arthritis - pyoderma gangrenosum - acne
Autoimmune lymphoproliferative syndrome

PSTPIP1 CASP10
FAS
FASLG
NRAS
PRKCD


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PSTPIP1
(0.96)
FASLG



Citations in the biomedical literature:


Pyogenic arthritis - pyoderma gangrenosum - acne
PSTPIP1
Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD



Pyogenic arthritis - pyoderma gangrenosum - acne
Autoimmune lymphoproliferative syndrome

Synonym(s):
- FRA
- Familial recurrent arthritis
- PAPA syndrome

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
3 OMIM references -
1 MeSH reference: D056735

Pyogenic arthritis - pyoderma gangrenosum - acne

Very frequent
- Acne / acnea
- Arthritis / synovitis / synovial proliferation
- Asthenia / fatigue / weakness
- Autosomal dominant inheritance
- Chronic skin infection / ulcerations / ulcers / cancrum
- Fever / chilling
- Pustula / pustulosis
- Restricted joint mobility / joint stiffness / ankylosis

Frequent
- Articular / joint pain / arthralgia
- Lymphadenopathy / polyadenopathies
- Monoclonal immunoglobulins / gammapathy / dysglobulinemia

Occasional
- Biological inflammatory syndrome / increased erythrocyte sedimentation rate / CRP
- Bone marrow failure / pancytopenia
- Functional colopathy / irritable bowel syndrome
- Furuncle / cutaneous abscess / hidrosadenitis suppurativa
- Insulin-dependent / type 1 diabetes
- Myositis
- Proteinuria


Autoimmune lymphoproliferative syndrome

(no data available)