Disease-gene associations mined from literature

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,  DOID:0060408,  chromosome 19q1311 deletion syndrome,  chromosome 19q13.11 deletion disease,  chromosome 19q13.11 deletion disorder ...