autosomal dominant intellectual developmental disorder 39

Term ID

DOID:0070069

Synonyms

• autosomal dominant mental retardation 39
• autosomal dominant non-syndromic intellectual disability 39
• MRD39

Definition

An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3. https://www.ncbi.nlm.nih.gov/pubmed/23033978

References

• OMIM:616521

Ontology

Human Disease   ( DOID:0070069 )