| UMLS CUI | C0032897 |
| UMLS Term | Prader-Willi Syndrome |
| MeSH ID | D011218 |
| MeSH Term | Prader-Willi Syndrome |
| Disease Classes |
Nervous System Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities Nutritional and Metabolic Diseases |
| Gene Symbol | Description | Entrez ID | Uniprot ID | Chromosomal Location |
|---|---|---|---|---|
|
SNRPN |
small nuclear ribonucleoprotein polypeptide N |
6638 |
P63162 |
chr15: 24,823,637-24,978,723 |