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6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
11 OMIM references -
3 associated genes
No signs/symptoms info
Situs ambiguus
Familial cerebral saccular aneurysm

ACVR2B COL3A1
CCDC11 ENG
CFC1 TGFBR3
LEFTY2
NODAL
ZIC3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
ACVR2B
(0.72)
ENG



Citations in the biomedical literature:


Situs ambiguus
ACVR2B CCDC11 CFC1 LEFTY2 NODAL ZIC3

Familial cerebral saccular aneurysm
COL3A1 ENG TGFBR3



Situs ambiguus
Familial cerebral saccular aneurysm

Synonym(s):
- Incomplete situs inversus
- Partial situs inversus
- Situs ambiguous

Synonym(s):
- Familial berry aneurysm
- Familial intracranial saccular aneurysm

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant

External references:
No OMIM references
No MeSH references
External references:
11 OMIM references -
No MeSH references

No signs/symptoms info available.