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Collaborative Research
Diseases
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Metabolic disease
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Amino acid metabolism disease
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Inborn disorder of amino acid metabolism
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Inborn disorder of amino acid transport
Histidinuria due to a renal tubular defect
rare
Identifiers
MONDO:0009346
OMIM:235830
Orphanet:2158
Part of
Histidinemia
Inborn disorder of amino acid transport
Also known as
histidinuria-renal tubular defect syndrome
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