eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | prader willi syndrome |
| Comorbidity | 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. |
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