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Dictionary » Homocystinuria due to defect in methylation type cbl G
 

Homocystinuria due to defect in methylation type cbl G

Introduction: Homocystinuria due to defect in methylation type cbl G

Description of Homocystinuria due to defect in methylation type cbl G

Homocystinuria due to defect in methylation type cbl G (medical condition): An inherited organic acid disorder where an enzyme deficiency ...more »

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Homocystinuria due to defect in methylation (cbl g):
  »Introduction: Homocystinuria due to defect in methylation (cbl g)
  »Symptoms of Homocystinuria due to defect in methylation (cbl g)

Homocystinuria due to defect in methylation type cbl G: Related Topics

These medical condition or symptom topics may be relevant to medical information for Homocystinuria due to defect in methylation type cbl G:

Homocystinuria due to defect in methylation type cbl G: Rare Disease

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Homocystinuria due to defect in methylation type cbl G as a "rare disease".

Source - Orphanet

Homocystinuria due to defect in methylation type cbl G as a Disease

Homocystinuria due to defect in methylation type cbl G: Another name for Homocystinuria due to defect in methylation (cbl g) (or close medical condition association).
  »Introduction: Homocystinuria due to defect in methylation (cbl g)
  »Symptoms of Homocystinuria due to defect in methylation (cbl g)

Homocystinuria due to defect in methylation type cbl G: Related Diseases

Homocystinuria due to defect in methylation type cbl G: Homocystinuria due to defect in methylation type cbl G is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Homocystinuria due to defect in methylation type cbl G (Homocystinuria due to defect in methylation (cbl g))

Some of the symptoms of Homocystinuria due to defect in methylation type cbl G incude:

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