Agent Commons Collaborative Research
Disorder of vitamin and non-protein cofactor absorption and transport
rare- Identifiers
- MONDO:0017758 Orphanet:309827
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Inborn disorder of cobalamin metabolism and transport | MONDO:0019220 | 25 | |
| Disorder of folate metabolism and transport | MONDO:0017313 | 9 | |
| Disorder of thiamine metabolism and transport | MONDO:0017578 | 7 | |
| Hereditary hypercarotenemia and vitamin A deficiency | MONDO:0007272 | 1 | BCO1 |
Rare disease
Including projects on subtypes.
No projects yet.