ODCs

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

PROTEIN INTERACTIONS: 1

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

Acute necrotizing encephalopathy of childhood

Familial infantile bilateral striatal necrosis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	RANBP2	(0.52)	NUP62

Citations in the biomedical literature:

Acute necrotizing encephalopathy of childhood		Familial infantile bilateral striatal necrosis
	Synonym(s): - ANEC - Isolated ANE - Isolated acute necrotizing encephalopathy		Synonym(s): - Familial IBSN - Familial infantile striatonigral degeneration - Familial infantile striatonigral necrosis

	Classification (Orphanet): - Rare infectious disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		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 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.