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KIF22A gene on chromosome 16p11.2 that encodes a microtubule- and DNA-binding, kinesin-like protein involved in spindle formation and chromosome movement during mitosis and meiosis.
A rare genetic disease in which patients are born with calloused skin on the hands and feet, scaly plaques on the arms and face, corneal inflammation, and deafness. The hearing impairment can be treated with cochlear implants.