Hyperhomocysteinemia

Condition in which the plasma levels of homocysteine and related metabolites are elevated (>13.9 μmol/l). Hyperhomocysteinemia can be familial or acquired. Development of the acquired hyperhomocysteinemia is mostly associated with vitamins B and/or folate deficiency (e.g., PERNICIOUS ANEMIA, vitamin malabsorption). Familial hyperhomocysteinemia often results in a more severe elevation of total homocysteine and excretion into the urine, resulting in HOMOCYSTINURIA. Hyperhomocysteinemia is a risk factor for cardiovascular and neurodegenerative diseases, osteoporotic fractures and complications during pregnancy.

Also Known As:

Hyperhomocysteinemias

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Amino Acid Metabolism: 1
      - Hyperhomocysteinemia: 3797
Nutritional and Metabolic Diseases: 15
- Metabolic Diseases: 10142
  - Inborn Errors Metabolism: 1162
    - Inborn Errors Amino Acid Metabolism: 1
      - Hyperhomocysteinemia: 3797
  - Malabsorption Syndromes: 639
    - Hyperhomocysteinemia: 3797
- Nutrition Disorders: 404
  - Malnutrition: 20403
    - Deficiency Diseases: 514
      - Avitaminosis: 1294
        Vitamin B Deficiency: 65
        Hyperhomocysteinemia: 3797

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Disease

Drug/Important Bio-Agent (IBA)