Intellectual disability, autosomal recessive 47

Definition

Any autosomal recessive non-syndromic intellectual disability in which the cause of the disease is a mutation in the FMN2 gene.

Also known as autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2, FMN2 autosomal recessive non-syndromic intellectual disability, intellectual developmental disorder, autosomal recessive 47, intellectual disability, autosomal recessive 47, intellectual disability, autosomal recessive type 47, mental retardation, autosomal recessive type 47 — per MONDO

Also identified as

• DOID 0081211 per MONDO
• OMIM 616193 per MONDO
• UMLS C4015444 per MONDO