Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition 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. Disease data Classification Disease Synonyms Congenital folate malabsorption Wrodzone złe wchłanianie kwsau foliowego ORPHA code 90045 OMIM code 229050 ICD10 code D52.8 ICD11 code - *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl