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Congenital valvular dysplasia
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Growth retardation-mild developmental delay-chronic hepatitis syndrome
1 associated gene
No signs/symptoms info
Congenital valvular dysplasia
Growth retardation-mild developmental delay-chronic hepatitis syndrome

FLNA
(UniProt - OMIM)
 SH2B3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNA
(0.77)
SH2B3


Citations in the biomedical literature:


Congenital valvular dysplasia
FLNA
Growth retardation-mild developmental delay-chronic hepatitis syndrome
SH2B3



Congenital valvular dysplasia
Growth retardation-mild developmental delay-chronic hepatitis syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare surgical cardiac disease
Classification (Orphanet):
- Rare genetic disease
- Rare hepatic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.