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

Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis

Parkinsonim due to ATP13A2 deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	LRP6	(0.72)	ATP13A2

Citations in the biomedical literature:

Coronary artery disease - hyperlipidemia - hypertension - diabetes - osteoporosis		Parkinsonim due to ATP13A2 deficiency
	Synonym(s): (no synonyms)		Synonym(s): - CLN12 disease

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: no data available Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

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

No signs/symptoms info available.