ORPHA:79273
Hereditary coproporphyria
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:79273 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Abdominal pain
- Elevated urinary delta-aminolevulinic acid
- Abnormal circulating porphyrin concentration
- Atypical scarring of skin
- Nausea
- Distal muscle weakness