Cytoscape Web
Click node...

Familial cerebral saccular aneurysm
11 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Nodulosis-arthropathy-osteolysis syndrome
2 OMIM references -
2 associated genes
No signs/symptoms info
Familial cerebral saccular aneurysm
Nodulosis-arthropathy-osteolysis syndrome

COL3A1
(UniProt - OMIM)
 MMP14
(UniProt - OMIM)
ENG
(UniProt - OMIM)
 MMP2
(UniProt - OMIM)
TGFBR3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ENG
(0.49)
MMP14


Citations in the biomedical literature:


Familial cerebral saccular aneurysm
COL3A1 ENG TGFBR3
Nodulosis-arthropathy-osteolysis syndrome
MMP14 MMP2



Familial cerebral saccular aneurysm
Nodulosis-arthropathy-osteolysis syndrome

Synonym(s):
- Familial berry aneurysm
- Familial intracranial saccular aneurysm
Synonym(s):
- Multicentric osteolysis - nodulosis - arthropathy
- NAO syndrome
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
11 OMIM references -
No MeSH references
External references:
2 OMIM references -
No MeSH references
No signs/symptoms info available.