P P- P0 P1 P2 P3 P4 P5 P6 P7 P8 P9 PA PB PC PD PE PF PG PH PI PK PL PM PN PO PP PQ PR PS PT PU PV PW PX PY
purine/pyrimidine metabolism disorder
[condition in which there is a deviation or interruption in the processing of purine or pyrmidine in the body: its absorption, transport, storage, and utilization. ( CSP )]
UMLS (CSP) C0034139- Disease or Syndrome
Relation/PAR: Congenital Metabolic Disorder
Relation/CHD: Gicht
hypoxanthine guanine phosphoribosyltransferase deficiency
orotate phosphoribosyltransferase deficiency
Gicht
hypoxanthine guanine phosphoribosyltransferase deficiency
hypoxanthine guanine phosphoribosyltransferase deficiency
orotate phosphoribosyltransferase deficiency
Gicht
hypoxanthine guanine phosphoribosyltransferase deficiency
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