| Label | Id | |
|---|---|---|
| LNS | 10298 | |
| HG-PRT deficiency | 10298 | |
| Hprt1 deficiency | 10298 | |
| Lesch-Nyhan syndrome | 10298 | |
| X-linked hyperuricemia | 10298 | |
| HPRT deficiency, neurologic variant | 10298 | |
| Lesch - Nyhan syndrome | 10298 | |
| HPRT complete deficiency | 10298 | |
| hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome]) | 10298 | |
| X-linked hyperuricemia (disorder) [ambiguous] | 10298 | |
| Lesch Nyhan disease | 10298 | |
| hypoxanthine-guanine-phosphoribosyltransferase deficiency | http://purl.obolibrary.org/obo/MONDO_0010298 | |
| deficiency of IMP pyrophosphorylase | 10298 | |
| Lesch-Nyhan syndrome; LNS | http://purl.obolibrary.org/obo/MONDO_0010298 | |
| HPRT deficiency, complete | 10298 |