ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Periventricular nodular heterotopia

Autosomal recessive limb-girdle muscular dystrophy type 2J


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA	(0.63)	TTN

Citations in the biomedical literature:

Periventricular nodular heterotopia		Autosomal recessive limb-girdle muscular dystrophy type 2J
	Synonym(s): (no synonyms)		Synonym(s): - LGMD2J

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	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.