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

Congenital valvular dysplasia

Lethal congenital contracture syndrome type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.55)	ERBB3

Citations in the biomedical literature:

Congenital valvular dysplasia		Lethal congenital contracture syndrome type 2
	Synonym(s): (no synonyms)		Synonym(s): - LCCS2 - Multiple contracture syndrome, Israeli-Bedouin type

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - 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: childhood Average age of death: - Type of inheritance: sporadic		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.