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Dictionary » Homocystinuria due to defect in methylation type cbl E
 

Homocystinuria due to defect in methylation type cbl E

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

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

Homocystinuria due to defect in methylation type cbl E: 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 E as a "rare disease".

Source - Orphanet

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

Homocystinuria due to defect in methylation type cbl E: Another name for Homocytsinuria due to defect in methylation cbl e (or close medical condition association).
  »Introduction: Homocytsinuria due to defect in methylation cbl e

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

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

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