Human genes for chromosome 14q11-q22 deletion syndrome
Chromosome 14q11-q22 deletion syndrome [DOID:0060392]
A chromosomal deletion syndrome that is characterized by microcephaly, dysmorphic facies, psychomotor delay and failure to thrive, has_material_basis_in isolated cases of partial deletion of the long arm of chromosome 14.
Synonyms: chromosome 14q11-q22 deletion syndrome, chromosome 14q11q22 deletion syndrome, chromosome 14q11-q22 deletion disease, chromosome 14q11-q22 deletion disorder, DOID:0060392 ...