Disease Description

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