ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal dominant keratitis

Spinocerebellar ataxia type 17


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PAX6	(0.88)	TBP

Citations in the biomedical literature:

Autosomal dominant keratitis		Spinocerebellar ataxia type 17
	Synonym(s): - Hereditary keratitis		Synonym(s): - HDL4 - Huntington disease-like 4 - SCA17

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

	External references: 1 OMIM reference - 1 MeSH reference: C537022		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.