Human genes for chromosome 19q13.11 deletion syndrome
Chromosome 19q13.11 deletion syndrome [DOID:0060408]
A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties.
Synonyms: chromosome 19q13.11 deletion syndrome, chromosome 19q1311 deletion syndrome, chromosome 19q13.11 deletion disease, chromosome 19q13.11 deletion disorder, DOID:0060408 ...