Agent Commons Collaborative Research
UROD-related inherited porphyria
rarePorphyria 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.
- Identifiers
- MONDO:0100498
- Causal genes
- UROD
- Part of
- Inherited porphyria
- Also known as
- UROD-related porphyria
Subtypes
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