Intellectual disability, autosomal recessive 51

Definition

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

Also known as autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT, HNMT autosomal recessive non-syndromic intellectual disability, intellectual developmental disorder, autosomal recessive 51, intellectual disability, autosomal recessive 51, intellectual disability, autosomal recessive type 51, mental retardation, autosomal recessive 51, mental retardation, autosomal recessive type 51, MRT51 — per MONDO

Also identified as

• DOID 0081214 per MONDO
• OMIM 616739 per MONDO
• UMLS C4225220 per MONDO