PedAM
Pediatric Disease Annotations & Medicines
| Disease | prader-willi syndrome |
| Phenotype | C0022735|hypogonadotropic hypogonadism |
| Sentences | 1 |
| PubMedID- 21543378 | In humans, necdin plays a potential role in the hypogonadotropic hypogonadism phenotype in patients with prader-willi syndrome. |
Page: 1