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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Severe combined immunodeficiency due to CORO1A deficiency
Aneurysm - osteoarthritis syndrome

CORO1A SMAD3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CORO1A
(0.63)
SMAD3



Citations in the biomedical literature:


Severe combined immunodeficiency due to CORO1A deficiency
CORO1A
Aneurysm - osteoarthritis syndrome
SMAD3



Severe combined immunodeficiency due to CORO1A deficiency
Aneurysm - osteoarthritis syndrome

Synonym(s):
- SCID due to CORO1A deficiency
- SCID due to coronin-1A deficiency
- Severe combined immunodeficiency due to coronin-1A deficiency

Synonym(s):
- AOS
- Loeys-Dietz syndrome with osteoarthritis

Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (Orphanet):
- Rare circulatory system disease
- Rare genetic disease
- Rare surgical thoracic disease
- Rare systemic or rheumatologic 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: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.