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Periventricular nodular heterotopia
5 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
1 OMIM reference -
1 associated gene
No signs/symptoms info
Periventricular nodular heterotopia
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations

ARFGEF2
(UniProt - OMIM)
 BRCA2
(UniProt - OMIM)
ERMARD
(UniProt - OMIM)
FLNA
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNA
(0.79)
BRCA2


Citations in the biomedical literature:


Periventricular nodular heterotopia
ARFGEF2 ERMARD FLNA
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations
BRCA2



Periventricular nodular heterotopia
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare oncologic disease
- Rare renal disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: unknown
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
5 OMIM references -
1 MeSH reference: D054091
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.