- Autosomal recessive hereditary disorder
- Cardiovascular system hereditary disorder (disorder)
- Congenital cardiovascular disorder (disorder)
- Congenital cataract
- Hereditary disorder of musculoskeletal system
- Hereditary disorder of the visual system
- Hypertrophic mitochondrial cardiomyopathy (disorder)
- Mitochondrial myopathy (disorder)
Name: Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
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- Sengers syndrome
- Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder)
- Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
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Concept ID: 717812000- Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder)
- Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
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Read Codes:
ICD-10 Codes: Q878