Genetics & Inherited Metabolic Diseases
The Division of Genetics and Inherited Metabolic Diseases unites two areas of deep expertise to deliver comprehensive care for children with rare and complex conditions. For learners and faculty, our division offers a collaborative environment emphasizing clinical expertise and research discovery.
As a learner, you'll gain hands-on experience across multidisciplinary clinics serving patients of all ages, including skeletal dysplasia, autism spectrum disorder, cardiovascular genetics, complex care and adult genetics. The division welcomes genetic counseling students, medical students, residents and fellows into both inpatient and outpatient settings every year. An inpatient consultation service runs around the clock, giving you real-world exposure from day one.
Our faculty lead and participate in laboratory and clinical studies focused on lipid metabolism, bone disease and rare inherited conditions. William Rizzo, MD, serves as principal investigator for the National Institutes of Health-funded Sterol and Isoprenoid Diseases Consortium, which conducts clinical investigations for conditions including Smith-Lemli-Opitz Syndrome, Sjögren-Larsson Syndrome and Cerebrotendinous Xanthomatosis.
The Medical Genetics residency program within our division continues to grow, graduating two fellows in 2023.
Meet Our Chief
Get to know Lois J. Starr, MD, PhD, chief of Genetics.