ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1

16 OMIM references -
4 associated genes
No signs/symptoms info

3-hydroxy-3-methylglutaryl-CoA synthase deficiency

Early-onset autosomal dominant Alzheimer disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HMGCS2	(0.56)	APP

Citations in the biomedical literature:

3-hydroxy-3-methylglutaryl-CoA synthase deficiency		Early-onset autosomal dominant Alzheimer disease
	Synonym(s): - HMG-CoA synthase deficiency		Synonym(s): - EOFAD - Early-onset familial autosomal dominant Alzheimer disease - Familial Alzheimer disease

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - No MeSH references		External references: 16 OMIM references - No MeSH references

3-hydroxy-3-methylglutaryl-CoA synthase deficiency
	Very frequent - Hypoglycemia - Metabolic anomalies - Organic acid metabolism anomalies - Seizures / epilepsy / absences / spasms / status epilepticus - Storage liver disease
Early-onset autosomal dominant Alzheimer disease
(no data available)