ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
20 signs/symptoms

Succinyl-CoA:3-ketoacid CoA transferase deficiency

Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	OXCT1	(0.49)	SUCLA2

Citations in the biomedical literature:

Succinyl-CoA:3-ketoacid CoA transferase deficiency		Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
	Synonym(s): - OXCT1 deficiency - SCOT deficiency - Succinyl-CoA acetoacetate transferase deficiency - Succinyl-CoA:3-oxoacid CoA transferase deficiency		Synonym(s): - Booth-Haworth-Dilling syndrome - Mitochondrial encephalomyopathy - aminoacidopathy - mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease		Classification (Orphanet): - Inborn errors of metabolism - 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: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: child / adolescent Type of inheritance: mitochondrial inheritance

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

Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
	Very frequent - Abnormal ERG / electroretinogram / electroretinography - Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase - Abnormal VEP / Visual evoked potential - Aminoacid metabolism anomalies / aminoaciduria - Areflexia / hyporeflexia - Ataxia / incoordination / trouble of the equilibrium - Central deafness / hearing loss - Dilated cerebral ventricles without hydrocephaly - Hirsutism / hypertrichosis / Increased body hair - Intellectual deficit / mental / psychomotor retardation / learning disability - Intracranial / cerebral calcifications - Microcephaly - Mild visual loss / impaired visual acuity - Muscle hypotrophy / atrophy / dystrophy / agenesis / amyotrophy - Nerve conduction abnormality - Psychic / behavioural troubles - Ptosis - Seizures / epilepsy / absences / spasms / status epilepticus - Short stature / dwarfism / nanism - Wasted (excluding lipodystrophy) / poorly muscled build / cachexy
Succinyl-CoA:3-ketoacid CoA transferase deficiency
(no data available)