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Repository for lectin-assisted multimodality data
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MIRAGE
hereditary folate malabsorption
Summary
- Synonym
-
- congenital defect of folate absorption
- congenital folate malabsorption
- 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.
- Super Class
- autosomal recessive disease vitamin metabolic disorder
External Links
- Disease Ontology
- DOID:0111678
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- ORDO
- GARD
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q96NT5 | Proton-coupled folate transporter |
