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Pronunciation: klō-rid-ō-rē′ă
Definition: A congenital autosomal recessive condition of intestinal chloride malabsorption, with intrauterine and life-long diarrhea. MIM #214700 (as chloride diarrhea, familial); gene map locus 7q22-q31.1
Synonym(s): congenital chloride diarrhea, congenital chloridorrhea
[chloride + -rrhea]
Examples: glitazone, GI cocktail, etc.
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