LD50.04LeafLevel 6
Mosaicism, 45, X or other cell line with abnormal sex chromosome
**Definition:** A disease caused by embryonic fusion or the structural mutation of a sex chromosome early in embryonic development, resulting in a subset of cells in the body having one normal copy of the X chromosome and one abnormal sex chromosome. This disease may present with short stature, sexual organ dysfunction, or may be asymptomatic.
GET
/api/v1/systems/icd_11/nodes/LD50.04Cross-system equivalences0
No cross-system equivalences mapped for this node.