Human genes for chromosome 16p12.2-p11.2 deletion syndrome
Chromosome 16p12.2-p11.2 deletion syndrome [DOID:0060400]
A chromosomal deletion syndrome that has_material_basis_in a chromosome 16p12.2-p11.2 deletion and that is characterized by dysmorphic facial features, feeding difficulties, recurrent ear infections, developmental delay, and cognitive impairment.
Synonyms: chromosome 16p12.2-p11.2 deletion syndrome, chromosome 16p122p112 deletion syndrome, chromosome 16p12.2-p11.2 deletion disease, chromosome 16p12.2-p11.2 deletion disorder, DOID:0060400 ...