Prev Term: histidine decarboxylase
Next Term: histiocyte
histidinemia
Broader Terms:
inborn aminoacid metabolism disorder
Broader Terms:
mental retardation
Related Terms:
autosomal recessive trait
Related Terms:
speech disorder
Scope Note:
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.
Term Number:
1849-0778
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