CRBN

cereblon
OMIM: 609262, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber CRBN in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Intellectual developmental disorder, autosomal recessive 2 MIM#607417

Amber CRBN in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review Unknown
Sources
  • Expert Review Amber
  • Genetic Health Queensland
Phenotypes
  • Mental retardation, autosomal recessive 2, MIM# 607417