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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autoimmune lymphoproliferative syndrome with recurrent infections
Progressive supranuclear palsy - progressive non fluent aphasia

CASP8 MAPT


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CASP8
(0.55)
MAPT



Citations in the biomedical literature:


Autoimmune lymphoproliferative syndrome with recurrent infections
CASP8
Progressive supranuclear palsy - progressive non fluent aphasia
MAPT



Autoimmune lymphoproliferative syndrome with recurrent infections
Progressive supranuclear palsy - progressive non fluent aphasia

Synonym(s):
- ALPS with recurrent infections

Synonym(s):
- PSP-AOS
- PSP-PNFA
- Progressive supranuclear palsy - apraxia of speech

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
- Rare oncologic disease
Classification (Orphanet):
- Rare eye 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: <1 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: adulthood
Average age of death: elderly
Type of inheritance: sporadic

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

No signs/symptoms info available.