AipOther Metabolites Mapped to 'Acute intermittent porphyria'HMDB0000051 (Ammonia) HMDB0000054 (Bilirubin) HMDB0000123 (Glycine) HMDB0000241 (Protoporphyrin IX) HMDB0000245 (Porphobilinogen) HMDB0000295 (Uridine 5'-diphosphate) HMDB0000570 (Coproporphyrin III) HMDB0000643 (Coproporphyrin I) HMDB0000692 (Fe2+) HMDB0000902 (NAD)
- HMDB0000692 (Fe2+)
- Acute intermittent porphyria
- a defect in this enzyme results in accumulation of 5-aminolevulinic acid or porphobilinogen in both urine and serum. most patients are completely free of symptoms between attacks.
- Parent Term
- Biochemical pathway
- Parent Definition
- A linked series of chemical reactions that occur in a defined order within or between organism cells, and lead to a known function or end product.