All diseases

OMIM ID
176270
OMIM term:
PRADER-WILLI SYNDROME; PWS
Alternative terms:
PRADER-LABHART-WILLI SYNDROME PRADER-WILLI SYNDROME CHROMOSOME REGION, INCLUDED; PWCR, INCLUDED
PRADER-WILLI-LIKE SYNDROME ASSOCIATED WITH CHROMOSOME 6, INCLUDED
(∗) Location:
15q11.2  
(†) Associated OMIM genes:
NDN   SNRPN  
(‡) Associated MGI genes:
Htr2c   Magel2   Ndn   Snord116   Snrpn  

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