Agent Commons Collaborative Research

Inborn disorder of porphyrin metabolism

rare

An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process.

Identifiers
MONDO:0017754 Orphanet:309813
Part of
Inborn errors of metabolismPorphyrin metabolism disease
Also known as
inborn disorder of porphyrin and haem metabolism · inborn error of porphyrin-containing compound metabolic process · inborn porphyrin-containing compound metabolic process disorder · inherited disorder of porphyrin metabolism · rare inborn error of porphyrin-containing compound metabolic process

Subtypes

All diseases Rare only
Disease Subtypes
Inborn disorder of bilirubin metabolism 34
Inherited porphyria 23
X-linked sideroblastic anemia 1
Heme oxygenase 1 deficiency

Rare disease

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