ODCs

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2 OMIM references -
5 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
15 signs/symptoms

Fatal infantile cytochrome C oxidase deficiency

Neuralgic amyotrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SCO2	(0.49)	SEPT9

Citations in the biomedical literature:

Fatal infantile cytochrome C oxidase deficiency		Neuralgic amyotrophy
	Synonym(s): - Fatal infantile COX deficiency - Fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency		Synonym(s): - Acute brachial plexus neuritis - Brachial plexus neuritis - Immune brachial plexus neuropathy - Mononeuritis multiplex with brachial predilection - Neuralgic shoulder amyotrophy - Serum neuritis - Winged scapula

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 6-9 / 10 000 Average age onset: adulthood Average age of death: normal Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

Neuralgic amyotrophy
	Very frequent - Abnormal EMG / electromyogram / electropmyography - Articular / joint pain / arthralgia - Muscle weakness / flaccidity - Neuritis / polyneuritis / multineuritis Frequent - Paresthesia / dysesthesia / hypoesthesia / anesthesia / numbness - Scapula structural / position anomaly / congenital elevation / Sprengel anomaly Occasional - Acrocyanosis / Raynaud's phenomenon / vasomotor disorders - Cleft lip and palate - Elocution disorders / dysarthria / dysphonia - Microstomia / little mouth - Peripheral neuropathy - Respiratory distress / dyspnea / respiratory failure / lung volume reduction - Round face - Short stature / dwarfism / nanism - Sleep and vigilance disorders
Fatal infantile cytochrome C oxidase deficiency
(no data available)