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Autoimmune lymphoproliferative syndrome
3 OMIM references -
5 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
1 associated gene
No signs/symptoms info
Autoimmune lymphoproliferative syndrome
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

CASP10
(UniProt - OMIM)
 DMD
(UniProt - OMIM)
FAS
(UniProt - OMIM)
FASLG
(UniProt - OMIM)
NRAS
(UniProt - OMIM)
PRKCD
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FASLG
(0.52)
DMD


Citations in the biomedical literature:


Autoimmune lymphoproliferative syndrome
CASP10 FAS FASLG NRAS PRKCD
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers
DMD



Autoimmune lymphoproliferative syndrome
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers

Synonym(s):
- ALPS
- Canale-Smith syndrome
- FAS deficiency
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
- Rare immune disease
- Rare oncologic disease
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: x-linked dominant
External references:
3 OMIM references -
1 MeSH reference: D056735
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.