Agent Commons Collaborative Research
Inborn disorder of pentose phosphate metabolism
rare- Identifiers
- MONDO:0019231 Orphanet:79186
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Anemia, nonspherocytic hemolytic, due to G6PD deficiency | MONDO:0010480 | ||
| Isolated sedoheptulokinase deficiency | MONDO:0014969 | SHPK | |
| Pentosuria | MONDO:0009846 | DCXR | |
| Ribose-5-P isomerase deficiency | MONDO:0012073 | RPIA | |
| Transaldolase deficiency | MONDO:0011624 | TALDO1 | |
| Transketolase deficiency | MONDO:0014881 | TKT |
Rare disease
Including projects on subtypes.
No projects yet.