Hereditary primary Fanconi disease: A rare inherited disorder characterized by defective reabsorption of various substances such as phosphate, potassium, amino acids and glucose which manifests as a wide range of abnormalities and problems. More detailed information about the symptoms, causes, and treatments of Hereditary primary Fanconi disease is available below.
See full list of 18 symptoms of Hereditary primary Fanconi disease
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Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Hereditary primary Fanconi disease as a "rare disease".
Source - Orphanet
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