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Dictionary » Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type
 

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type

Introduction: Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type

Description of Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type (medical condition): An inherited organic acid disorder where an enzyme deficiency (cbl G) impairs...more »

See also:

Methylcobalamin deficiency cbl G type:
  »Introduction: Methylcobalamin deficiency cbl G type
  »Symptoms of Methylcobalamin deficiency cbl G type

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type: Related Topics

These medical condition or symptom topics may be relevant to medical information for Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type:

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type as a Disease

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type: Another name for Methylcobalamin deficiency cbl G type (or close medical condition association).
  »Introduction: Methylcobalamin deficiency cbl G type
  »Symptoms of Methylcobalamin deficiency cbl G type

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type: Related Diseases

Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type: Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type is listed as a type of (or associated with) the following medical conditions in our database:

Symptoms of Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type (Methylcobalamin deficiency cbl G type)

Some of the symptoms of Homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type incude:

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