ODCs

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11 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial cerebral saccular aneurysm

Marfan syndrome type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ENG TGFBR3	(0.95) (0.86)	TGFBR2 TGFBR2

Citations in the biomedical literature:

Familial cerebral saccular aneurysm		Marfan syndrome type 2
	Synonym(s): - Familial berry aneurysm - Familial intracranial saccular aneurysm		Synonym(s): - Loeys-Dietz syndrome type 2 - MFS2

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare surgical thoracic disease - Rare systemic or rheumatologic disease

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

	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: any age Type of inheritance: autosomal dominant

	External references: 11 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.