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LCAD deficiency (medical condition): A rare inherited genetic condition where the body...more »
See also:
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency:
»Introduction: Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
»Symptoms of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
»Causes of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
These medical condition or symptom topics may be relevant to medical information for LCAD deficiency:
LCAD deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that LCAD deficiency, or a subtype of LCAD deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
LCAD deficiency: Another name for Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (or close medical condition association).
»Introduction: Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
»Symptoms of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
»Causes of Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
LCAD deficiency: LCAD deficiency is listed as a type of (or associated with) the following medical conditions in our database:
Some of the causes of LCAD deficiency are included in the list below:
Read more about causes of LCAD deficiency (Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency)
Some of the symptoms of LCAD deficiency incude:
See full list of 16 symptoms of LCAD deficiency (Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency)
These medical disease topics may be related to LCAD deficiency:
Source - NIH
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