ODCs

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

COMMON GENES: 1

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

Temperature-sensitive oculocutaneous albinism type 1

Ocular albinism with congenital sensorineural deafness

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

Citations in the biomedical literature:

Temperature-sensitive oculocutaneous albinism type 1		Ocular albinism with congenital sensorineural deafness
	Synonym(s): - OCA1-TS - TS OCA type 1		Synonym(s): - Waardenburg syndrome type 2 with ocular albinism

	Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Inborn errors of metabolism - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

No signs/symptoms info available.