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Histidinemia (medical condition): A metabolic disorder where there is a deficiency...more »
Histidinemia: autosomal recessive aminoacidopathy due to deficiency of histidine ammonia-lyase; characterized by accumulation of histidine in serum and urinary excretion of histidine and metabolites, but is usually benign; may cause mild central nervous system dysfunction.
These medical condition or symptom topics may be relevant to medical information for Histidinemia:
Histidinemia is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Histidinemia, or a subtype of Histidinemia,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Histidinemia as a "rare disease".
Source - Orphanet
Histidinemia: Histidinemia is listed as a type of (or associated with) the following medical conditions in our database:
These medical disease topics may be related to Histidinemia:
Source - NIH
Source - CRISP
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