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deficit prolidázy
Subject h. deficit prolidázy Subject h. Prolidase Deficiency Entry terms nedostatok prolidázy Scope note in English Rare autosomal recessive disorder of metabolism due to mutations in the prolidase gene. It is characterized by recurrent lower extremity skin ulcers, recurrent infections, and FACIES, often with INTELLECTUAL DISABILITY. 
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Number of the records: 1