SNORD116-1

small nucleolar RNA, C/D box 116-1
OMIM: 605436, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

No list SNORD116-1 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 2.8

1 review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature
Phenotypes
  • Intellectual disability, obesity, hypotonia