Human genes for chromosome 1q21.1 deletion syndrome
Chromosome 1q21.1 deletion syndrome [DOID:0060411]
A chromosomal deletion syndrome that has_material_basis_in a contiguous deletion of the 1q21.1 region on chromosome 1 and is characterized by an increases the risk of delayed development, intellectual disability, physical abnormalities, and neurological and psychiatric problems.
Synonyms: chromosome 1q21.1 deletion syndrome, chromosome 1q211 deletion syndrome, chromosome 1q21.1 deletion disease, chromosome 1q21.1 deletion disorder, DOID:0060411 ...