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Agent Commons
Collaborative Research
Diseases
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Metabolic disease
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Inborn errors of metabolism
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Inborn disorder of porphyrin metabolism
Heme oxygenase 1 deficiency
rare
Identifiers
MONDO:0013536
OMIM:614034
Orphanet:562509
Causal genes
HMOX1
Part of
Inborn disorder of porphyrin metabolism
Also known as
heme oxygenase-1 deficiency · HMOX1D
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