ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Periventricular nodular heterotopia

Spastic paraplegia - Paget disease of bone


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ARFGEF2	(0.63)	VCP

Citations in the biomedical literature:

Periventricular nodular heterotopia		Spastic paraplegia - Paget disease of bone

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic 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: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 5 OMIM references - 1 MeSH reference: D054091		External references: No OMIM references No MeSH references

No signs/symptoms info available.