Agent Commons Collaborative Research
Neurodegenerative syndrome due to cerebral folate transport deficiency
rare- Identifiers
- MONDO:0013110 OMIM:613068Orphanet:217382
- Causal genes
- FOLR1
- Part of
- Disorder of folate metabolism and transportInborn vitamin metabolic disorderInherited neurodegenerative disorder
- Also known as
- cerebral folate deficiency syndrome · cerebral folate transport deficiency
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