- ... deficiency. Learn more about the genes associated with 3-methylcrotonyl-CoA carboxylase deficiency MCCC1 MCCC2 Inheritance This condition is inherited in ...
- ... for energy. Health Conditions Related to Genetic Changes 3-methylcrotonyl-CoA carboxylase deficiency Many variants (also called mutations) in the MCCC1 ...
- ... for energy. Health Conditions Related to Genetic Changes 3-methylcrotonyl-CoA carboxylase deficiency Many variants (also called mutations) in the MCCC2 ...
- ... published></health-condition-summary><health-condition-summary ><name >3-methylcrotonyl-CoA carboxylase deficiency</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
- ... Glycogen storage disease type V MCC deficiency, see 3-methylcrotonyl-CoA carboxylase deficiency MCCD, see 3-methylcrotonyl-CoA carboxylase deficiency McCune- ...
- ... deficiency 3-M syndrome 3-MCC deficiency, see 3-methylcrotonyl-CoA carboxylase deficiency 3-methylcrotonyl-CoA carboxylase deficiency 3-methylcrotonylglycinuria, see ...
- ... topic><topic ><url >https://medlineplus.gov/genetics/condition/3-methylcrotonyl-coa-carboxylase-deficiency</url><title >3-methylcrotonyl-CoA carboxylase deficiency</title>< ...
- 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 ...
- 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 ...
- 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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