deficit dihydropyrimidindehydrogenázy
dědičná thymin-uracilurie
dihydropyrimidindehydrogenasa - deficience
dihydropyrimidindehydrogenasa - deficit
dihydropyrimidindehydrogenasa - nedostatek
Dihydropyrimidinuria
dihydropyrimidinurie
DPD Deficiency
Familial Pyrimidemia
Familial Pyrimidinemia
Hereditary Thymine-Uraciluria
nedostatek dihydropyrimidin dehydrogenázy
nedostatek DPD
Pyrimidinemia, Familial
pyrimidinémie
Thymine-Uraciluria, Hereditary
poruchy metabolismu purinů a pyrimidinů
Dihydropyrimidine Dehydrogenase Deficiency
MESH
(1) - MESH

Leschův-Nyhanův syndrom
Choreoathetosis Self-Mutilation Hyperuricemia Syndrome
Choreoathetosis Self-Mutilation Syndrome
Complete HGPRT Deficiency Disease
Complete HPRT Deficiency
Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency
Deficiency Disease, Complete HGPRT
Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase
Deficiency of Guanine Phosphoribosyltransferase
Deficiency of Hypoxanthine Phosphoribosyltransferase
deficit hypoxantin-guaninfosforibozyltransferázy
deficit hypoxantinfosforibozyltransferázy
HGPRT Deficiency
HGPRT Deficiency Disease, Complete
Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency
Hypoxanthine Guanine Phosphoribosyltransferase Deficiency
Hypoxanthine Phosphoribosyltransferase Deficiency
Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease
Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome
Juvenile Hyperuricemia Syndrome
kompletní deficit HPRT
kompletní deficit hypoxanthin-fosforibosyltransferázy
Lesch-Nyhan Disease
Primary Hyperuricemia Syndrome
Total HPRT Deficiency
Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency
X-Linked Hyperuricemia
X-Linked Primary Hyperuricemia
mentální retardace vázaná na chromozom X
metabolické nemoci mozku vrozené
poruchy metabolismu purinů a pyrimidinů
hypoxanthinfosforibosyltransferasa
Lesch-Nyhan Syndrome
MESH
(4) - MESH