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

COL3A1 CYP1B1
ENG MYOC
TGFBR3


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
COL3A1
(0.63)
MYOC



Citations in the biomedical literature:


Familial cerebral saccular aneurysm
COL3A1 ENG TGFBR3
Juvenile glaucoma
CYP1B1 MYOC



Familial cerebral saccular aneurysm
Juvenile glaucoma

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

Synonym(s):
(no synonyms)

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

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant

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

No signs/symptoms info available.