Cytoscape Web
Click node...


5 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 OMIM references -
2 associated genes
8 signs/symptoms
Periventricular nodular heterotopia
Hypoplastic left heart syndrome

ARFGEF2 GJA1
ERMARD NKX2-5
FLNA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FLNA
(0.63)
GJA1



Citations in the biomedical literature:


Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA
Hypoplastic left heart syndrome
GJA1 NKX2-5



Periventricular nodular heterotopia
Hypoplastic left heart syndrome

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare surgical cardiac 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: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: unknown

External references:
5 OMIM references -
1 MeSH reference: D054091
External references:
2 OMIM references -
1 MeSH reference: D018636

Hypoplastic left heart syndrome

Very frequent
- Hypoplastic left heart / ventricle
- Stillbirth / neonatal death

Frequent
- Hypoplastic aorta / coarctation / stenosis / anomaly / aortic arch interruption

Occasional
- Atrial septal defect / interauricular communication
- Maternal diabetes
- Mitral valve prolapse / incompetence / insufficiency / regurgitation / ring anomaly
- Patent ductus arteriosus
- Total / partial trisomy / duplication


Periventricular nodular heterotopia

(no data available)