Lesch-Nyhan syndrome (Q727436)
rare genetic syndrome
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aliases Complete hypoxanthine-guanine phosphoribosyltransferase deficiency
 HG-PRT deficiency
 Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder)
 Hypoxanthine-guanine phosphoribosyltransferase deficiency (disorder) [Ambiguous]
 Hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])
 Lesch - Nyhan syndrome
 Lesch-Nyhan syndrome (disorder)
 X-linked hyperuricemia (disorder) [Ambiguous]
 deficiency of IMP pyrophosphorylase
 hypoxanthine guanine phosphoribosyltransferase deficiency
 Lesch-Nyhan syndrome, LNS
 Hypoxanthine-guanine phosphoribosyltransferase deficiency
 X-linked hyperuricemia
 Hypoxanthine-guanine-phosphoribosyltransferase deficiency
 Lesch-Nyhan Disease
 LNS
description rare genetic syndrome

External Links
(P349) 00576013
(P486) D007926
(P492) 300322
(P493) 277.2
(P557) 7415
(P604) 001655
(P646) /m/047c68
(P665) H00194
(P668) NBK1149
(P672) C10.228.140.163.100.425
C10.597.606.360.455.625
C16.320.322.500.625
C16.320.400.525.625
C16.320.565.189.425
C16.320.565.798.594
C18.452.132.100.425
C18.452.648.189.425
C18.452.648.798.594
(P673) 1181356
(P699) DOID:1919
(P1296) 0037017
(P1417) science/Lesch-Nyhan-syndrome
(P1461) Lesch-Nyhan-Syndrome-(LNS)
(P1550) 510
(P2892) C0023374
(P4229) E79.1
(P4317) 7226
(P5270) MONDO_0010298
(P6366) 2777766392
(P7329) 5C55.01
(P7464) lesch-nyhan-syndrome
(P7807) 1886495906
(P9272) 8104
(P10283) C2777766392
(P11143) Lesch–Nyhan syndrome
(P11430) DI-01892
(P12385) sindrome-de-lesch-nyhan