ODCs

Click node...

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Neonatal Marfan syndrome

Congenital glaucoma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FBN1	(0.75)	MYOC

Citations in the biomedical literature:

Neonatal Marfan syndrome		Congenital glaucoma
	Synonym(s): - Neonatal MFS		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare surgical thoracic disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.