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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
29 OMIM references -
16 associated genes
No signs/symptoms info
Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal recessive nonsyndromic intellectual deficit

CASP8 CC2D1A
CRADD
CRBN
GRIK2
KIAA1033
LINS
MAN1B1
MED13L
MED23
NSUN2
PRSS12
ST3GAL3
TECR
TRAPPC9
TUSC3
ZC3H14


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CASP8
(0.52)
CRADD



Citations in the biomedical literature:


Autoimmune lymphoproliferative syndrome with recurrent infections
CASP8
Autosomal recessive nonsyndromic intellectual deficit
CC2D1A CRADD CRBN GRIK2 KIAA1033 LINS
MAN1B1 MED13L MED23 NSUN2 PRSS12 ST3GAL3
TECR TRAPPC9 TUSC3 ZC3H14



Autoimmune lymphoproliferative syndrome with recurrent infections
Autosomal recessive nonsyndromic intellectual deficit

Synonym(s):
- ALPS with recurrent infections

Synonym(s):
- NS-ARID

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (Orphanet):
- 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):
(no data available)

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

External references:
1 OMIM reference -
No MeSH references
External references:
29 OMIM references -
No MeSH references

No signs/symptoms info available.