myICD10.com Logo
smith-lemli-opitz syndrome

Medical Definition

Autosomal recessive disorder characterized by multiple congenital anomalies including microcephaly, mental retardation, unusual facies, and genital abnormalities; the biochemical defect is a lack of 7-dehydrocholesterol-delta-7-reductase, resulting in abnormally high levels of 7-dehydrocholesterol and low levels of cholesterol.
Related Codes (1)
Code
Description
Billable
Details
E78.72Smith-Lemli-Opitz syndrome

Rows per page

Page 1 of 1