National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Methemoglobinemia, beta-globin type


Other Names:
Autosomal dominant methemoglobinemia; Hereditary methemoglobinemia due to hemoglobin mutation; M hemoglobinopathy; Autosomal dominant methemoglobinemia; Hereditary methemoglobinemia due to hemoglobin mutation; M hemoglobinopathy; Hemoglobin M disease; Blue baby syndrome See More
Categories:
Subtypes:

These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • MedlinePlus was designed by the National Library of Medicine to help you research your health questions, and it provides more information about this topic.

In-Depth Information

  • Medscape Reference provides information on this topic. You may need to register to view the medical textbook, but registration is free.
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.

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