ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

Ocular albinism with congenital sensorineural deafness

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

MITF	(UniProt - OMIM)		APP	(UniProt - OMIM)
TYR	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MITF	(0.56)	APP

Citations in the biomedical literature:

Ocular albinism with congenital sensorineural deafness		Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Synonym(s): - Waardenburg syndrome type 2 with ocular albinism		Synonym(s): - HCHWA, Arctic type

	Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): (no data available)		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Very frequent - Autosomal dominant inheritance - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline
Ocular albinism with congenital sensorineural deafness
(no data available)