Disease association ontology term - MONDO:0009238 - hereditary folate malabsorption
Term summary
- ID
- MONDO:0009238
- Name
- hereditary folate malabsorption
- Ontology or CV name
- Disease association
- 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.
