ODCs

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

PROTEIN INTERACTIONS: 2

1 OMIM reference -
4 associated genes
No signs/symptoms info

Congenital valvular dysplasia

Myoclonus-dystonia syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	FLNA FLNA	(0.89) (0.49)	DRD2 DYT15

Citations in the biomedical literature:

Congenital valvular dysplasia		Myoclonus-dystonia syndrome
	Synonym(s): (no synonyms)		Synonym(s): - Alcohol-responsive dystonia - DYT11 - Hereditary essential myoclonus - Myoclonic dystonia

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare surgical cardiac 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: childhood Average age of death: - Type of inheritance: sporadic		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536096

No signs/symptoms info available.