ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial drusen

Benign paroxysmal torticollis of infancy

CFH	(UniProt - OMIM)		CACNA1A	(UniProt - OMIM)
EFEMP1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EFEMP1	(0.63)	CACNA1A

Citations in the biomedical literature:

Familial drusen		Benign paroxysmal torticollis of infancy
	Synonym(s): - DHRD - Dominant drusen - Dominant radial drusen - Doyne honeycomb retinal dystrophy - Malattia leventinese		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the eye and adnexa -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: normal Type of inheritance: sporadic

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

No signs/symptoms info available.