Lesch-Nyhan phenotype with normal HGPRT
MONDO:0010642Also known as: Lesch-Nyhan phenotype with normal HGPRT
1 clinical trial for this condition and its sub-types.
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Disease
(680)
Metabolic disease
(233)
Hereditary disease
(176)
Inborn errors of metabolism
(45)
Syndromic disease
(25)
Human disease
(14)
Disease of genetic or genomic mechanism
(2)
Inborn disorder of purine or pyrimidine metabolism
(1)
Lesch-Nyhan syndrome
(1)
Disease by body system or component
(0)