UROD-related inherited porphyria

MONDO:0100498

Porphyria caused by monoallelic and biallelic variants in UROD and presenting as a spectrum of disease (a semidominant inheritance pattern). Additionally, environmental factors almost always play a role in the disease. Monoallelic variants when exacerbated by environmental factors can result in episodic adult onset of photosensitivity. Biallelic variants that reduce WT enzyme activity <20% cause childhood onset of photosensitivity and sometimes liver damage.

Also known as: UROD-related porphyria

2 clinical trials for this condition and its sub-types.

Follow this condition to get notified about new trials

Sub-types

Broader categories

Sort by