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prader-willi syndrome

Medical Definition

Congenital neurobehavioral disorder characterized by rounded face, low forehead, almond shaped eyes, squinting, hypogonadism, hypotonia, insatiable appetite leading to obesity, and mental retardation; chromosomal disorder usually associated with a deletion of the proximal portion of the long arm of chromosome 15.
Related Codes (1)
Code
Description
Billable
Details
Q87.11Prader-Willi syndrome

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