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SNORD115@ - small nucleolar RNA, C/D box 115 cluster
Diseases list
- Role in the phenotype of Prader-Willi syndrome due to imprinting mutation
ORPHA:177910 - Role in the phenotype of Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1
ORPHA:177901 - Role in the phenotype of Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
ORPHA:177904

Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
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