ODCs

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

PROTEIN INTERACTIONS: 1

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

Familial infantile bilateral striatal necrosis

Acyl-CoA dehydrogenase 9 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MT-ATP6	(0.58)	ACAD9

Citations in the biomedical literature:

Familial infantile bilateral striatal necrosis		Acyl-CoA dehydrogenase 9 deficiency
	Synonym(s): - Familial IBSN - Familial infantile striatonigral degeneration - Familial infantile striatonigral necrosis		Synonym(s): - ACAD9 deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.