ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Marfan syndrome type 2

FG syndrome type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TGFBR2	(0.72)	MED12

Citations in the biomedical literature:

Marfan syndrome type 2		FG syndrome type 1
	Synonym(s): - Loeys-Dietz syndrome type 2 - MFS2		Synonym(s): - Opitz-Kaveggia syndrome

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare surgical thoracic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): (no data available)

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.