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Disease Ontology Browser
hereditary folate malabsorption (DOID:0111678)
Alliance: disease page
Synonyms: congenital defect of folate absorption; congenital folate malabsorption
Alt IDs: OMIM:229050, MESH:C562799, NCI:C156424, ORDO:90045, UMLS_CUI:C0342705
Definition: A vitamin metabolic disorder characterized by impaired intestinal folate absorption and impaired transport of folate into the central nervous system resulting in megaloblastic anemia, diarrhea, immune deficiency, infections, and neurologic deficits that has_material_basis_in homozygous or compound heterozygous mutation in the SLC46A1 gene on chromosome 17q11.2.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory