IU Health
David D. Weaver, MD

David D. Weaver, MD

IU Health

Medical & Molecular Genetics

4.3 out of 5 stars (51 ratings)
Accepting New Patients (Referral Required)
  • Biography
  • Locations
  • Specialties & Details
  • Ratings & Reviews
Biography

Dr. David D. Weaver specializes in Medical Genetics for Riley Medical & Molecular Genetics. Dr. Weaver earned his medical degree at the University of Oregon School of Medicine. He then completed an internship at Milwaukee County General Hospital a residency at the University of Oregon School of Medicine, and a fellowship at University of Washington School of Medicine in Seattle (Human Genetics) and University of Oregon School of Medicine (Metabolic Diseases).

Dr. Weaver currently has a rating of 4.4 stars out of 5 with over 50 ratings. Patients say that he is courteous, intelligent, and knowledgeable. In a recent five-star review, a patient remarked: "He's a very good doctor, he is courteous were very friendly and helpful and very thorough. Thank you."

Dr. Weaver's primary location is Riley Medical & Molecular Genetics, 575 Riley Hospital Dr, Indianapolis IN, 46202. He also sees patients at an office in Madison.

Locations
Specialties & Details

Specialties:

Medical & Molecular Genetics

Conditions & Treatments:

Clinical Genetics, Dysmorphology, Prenatal Diagnosis, Syndromology, Birth Defects And Inherited Disorders, Metabolism Disorders, Cystic Fibrosis Testing, Down Syndrome Screening, Dysmorphology, Genetic Counseling, Genetic Testing, Genetic Testing and Screening, Hemochromatosis Gene, Huntington's Disease Genetic Test, Molecular Cytogenetics, Sickle Cell Test, Syndromology, Tay-Sachs Test, Teratogen Consultation, Aortic Valve Stenosis in Newborns, Ashkenazi Jewish Genetic Panel, Atrial Septal Defect, Atrioventricular Septal Defect, Autosomal Recessive Disease, Bicuspid Aortic Valve, Birth Defects, Blood Clotting Disorders, Bone Dysplasia, Carnitine Deficiency, Chromosomal Abnormalities, Coarctation of the Aorta, Color Blindness, Congenital Heart Defects, Congenital Heart Disease, Connective Tissue Disorders, Cystic Fibrosis, Developmental Delay, Disorders of Sexual Development, Down Syndrome, Factor V Leiden, Fetal Alcohol Spectrum Disorders, Genetic Conditions, Genetic Heart Disease, Hirschsprung's Disease, Hypophosphatasia, Hypoplastic Left Heart Syndrome, Inherited Disorders, Klinefelter Syndrome, Lysosomal Storage Disorders, Malignant Hyperthermia, Marfan Syndrome, Osteogenesis Imperfecta, Patent Ductus Arteriosus, Patent Foramen Ovale, Prader Willi Syndrome, Pulmonary Valve Stenosis, Spina Bifida, Tetralogy of Fallot, Tricuspid Atresia, Turner Syndrome, Vascular Ehlers-Danlos Syndrome, Ventricular Septal Defect, Chromosomal Deletions, Chromosomal Duplications

Education

School of Medicine:

University of Oregon School of Medicine

Internship:

Milwaukee County General Hospital, Milwaukee, WI

Residency:

University of Oregon School of Medicine

Fellowship:

University of Washington School of Medicine in Seattle (Human Genetics); University of Oregon School of Medicine (Metabolic Diseases)

Hospitals & Affiliations

Hospital Privileges:

IU Health Methodist/IU Health University, Riley Hospital for Children at IU Health

Physician Group:

IU Health Physicians

Research

Research Publications
* Information provided by PubMed
Ratings & Reviews