Intellectual disability, autosomal recessive 2

Definition

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the CRBN gene.

Also known as autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN, CRBN autosomal recessive non-syndromic intellectual disability, intellectual disability, autosomal recessive 2, intellectual disability, autosomal recessive type 2, mental retardation, autosomal recessive type 2 — per MONDO

Also identified as

• DOID 0081178 per MONDO
• MESH C564404 per MONDO
• OMIM 607417 per MONDO
• UMLS C1843942 per MONDO