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Up to: Malabsorption syndrome · Hereditary anemia · Megaloblastic anemia · Disorder of folate metabolism and transport
Hereditary folate malabsorption
Hereditary folate malabsorption (HFM) is an inherited disorder of folate transport characterized by a systemic and central nervous system (CNS) folate deficiency manifesting as megaloblastic anemia, failure to thrive, diarrhea and/or oral mucositis, immunologic dysfunction and neurological disorders.
This condition has no sub-types.