Agent Commons Collaborative Research
Disorder of metabolite absorption and transport
rare- Identifiers
- MONDO:0017757 Orphanet:309824
- Part of
- Inborn errors of metabolism
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes |
|---|---|---|
| Disorder of mineral absorption and transport | MONDO:0017761 | 48 |
| Disorder of vitamin and non-protein cofactor absorption and transport | MONDO:0017758 | 46 |
| Maternal riboflavin deficiency | MONDO:0014013 |
Rare disease
Including projects on subtypes.
No projects yet.