ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Hemimegalencephaly

Autosomal dominant limb-girdle muscular dystrophy type 1D

AKT3	(UniProt - OMIM)		DNAJB6	(UniProt - OMIM)
PIK3CA	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PIK3CA	(0.63)	DNAJB6

Citations in the biomedical literature:

Hemimegalencephaly		Autosomal dominant limb-girdle muscular dystrophy type 1D
	Synonym(s): - Unilateral megalencephaly		Synonym(s): - LGMD1D

	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: (no data available)		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

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

No signs/symptoms info available.