UDP-Galactose-4-epimerase deficiency: A condition which is characterised by a mutation in the UDP-galactose-4-epimerase gene. More detailed information about the symptoms, causes, and treatments of UDP-Galactose-4-epimerase deficiency is available below.
See full list of 11 symptoms of UDP-Galactose-4-epimerase deficiency
Read more about complications of UDP-Galactose-4-epimerase deficiency.
Read more about causes of UDP-Galactose-4-epimerase deficiency.
Research the causes of these diseases that are similar to, or related to, UDP-Galactose-4-epimerase deficiency:
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Read more about Misdiagnosis and UDP-Galactose-4-epimerase deficiency
Types of UDP-Galactose-4-epimerase deficiency
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UDP-Galactose-4-epimerase deficiency is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that UDP-Galactose-4-epimerase deficiency, or a subtype of UDP-Galactose-4-epimerase deficiency,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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