ODCs

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

PROTEIN INTERACTIONS: 1

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

Familial exudative vitreoretinopathy

Huntington disease-like 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ZNF408	(0.68)	PRNP

Citations in the biomedical literature:

Familial exudative vitreoretinopathy		Huntington disease-like 1
	Synonym(s): - Criswick-Schepens syndrome - FEVR		Synonym(s): - Early onset prion disease with prominent psychiatric features - HDL1

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: any age Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 5 OMIM references - 1 MeSH reference: C536382		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.