/neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

Rare Disease

MONDO:0014562

Also Known As

COQ4-related neonatal encephalomyopathycoenzyme Q10 deficiency, primary, type 7COQ10D7coenzyme Q10 deficiency, primary, 7primary coenzyme Q10 deficiency 7

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

Checking for content...

Associated Genes

COQ4 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

Related Diseases

coenzyme Q10 deficiency, primary, 1

MONDO:0011829

Rare

autosomal recessive ataxia due to ubiquinone deficiency

MONDO:0012784

Rare

familial steroid-resistant nephrotic syndrome with sensorineural deafness

MONDO:0013836

Rare

deafness-encephaloneuropathy-obesity-valvulopathy syndrome

MONDO:0013837

Rare

coenzyme Q10 deficiency, primary, 3

MONDO:0013838

Rare

encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome

MONDO:0013840

Rare

← Back to All Diseases

neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome

Also Known As

Patient-Friendly Information

Associated Genes

External Resources

OMIM

Orphanet

GARD

Related Diseases