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23 results
  1. ... deficiency. Learn more about the genes associated with 3-methylcrotonyl-CoA carboxylase deficiency MCCC1 MCCC2 Inheritance This condition is inherited in ...
  2. ... for energy. Health Conditions Related to Genetic Changes 3-methylcrotonyl-CoA carboxylase deficiency Many variants (also called mutations) in the MCCC1 ...
  3. ... for energy. Health Conditions Related to Genetic Changes 3-methylcrotonyl-CoA carboxylase deficiency Many variants (also called mutations) in the MCCC2 ...
  4. ... published></health-condition-summary><health-condition-summary ><name >3-methylcrotonyl-CoA carboxylase deficiency</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
  5. ... Glycogen storage disease type V MCC deficiency, see 3-methylcrotonyl-CoA carboxylase deficiency MCCD, see 3-methylcrotonyl-CoA carboxylase deficiency McCune- ...
  6. ... deficiency 3-M syndrome 3-MCC deficiency, see 3-methylcrotonyl-CoA carboxylase deficiency 3-methylcrotonyl-CoA carboxylase deficiency 3-methylcrotonylglycinuria, see ...
  7. ... topic><topic ><url >https://medlineplus.gov/genetics/condition/3-methylcrotonyl-coa-carboxylase-deficiency</url><title >3-methylcrotonyl-CoA carboxylase deficiency</title>< ...
  8. Genetic brain disorders affect the development and function of the brain. Some are inherited, some are caused by exposure, and others are both. ... A genetic ...
  9. Your newborn infant has screening tests before leaving the hospital. Get the facts about these tests and what you should expect. ... Your newborn infant has screening ...
  10. Disorders like phenylketonuria (PKU) and maple syrup urine disease cause problems with how your body uses proteins. Learn more about them. ... Metabolism is the process ...
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