Disease #03238 (NCFTD (neurodegeneration due to cerebral folate deficiency), OMIM:613068)
| Official abbreviation |
NCFTD |
| Name |
neurodegeneration due to cerebral folate deficiency |
| OMIM ID |
613068 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
FOLR1 |
| Associated tissues |
- |
| Disease features |
autosomal recessive |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2025-11-07 09:10:39 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|