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Hereditary folate malabsorption

MONDO:0009238

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.

Also known as: congenital folate malabsorption, congenital defect of folate absorption, folate malabsorption, hereditary, folic acid transport defect

10 clinical trials for this condition and its sub-types, 0 tagged with Hereditary folate malabsorption itself.

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↑ Malabsorption syndrome (118) ↑ Hereditary anemia (13) ↑ Megaloblastic anemia (9) ↑ Disorder of folate metabolism and transport (2)

Including sub-types (10) Tagged with Hereditary folate malabsorption (0)

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