Melissa D. Lah, MD

Melissa D. Lah, MD

Accepting New Patients (Referral Required)

Pediatrics | Medical & Molecular Genetics

IU Health
Accepting New Patients (Referral Required)

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  • Locations
  • Specialties & Details
Locations Slice
  • Riley Medical & Molecular Genetics

Specialty Care

Riley Medical & Molecular Genetics

1002 Wishard Blvd
Indianapolis, IN 46202



Riley Medical & Molecular Genetics

4935 W Arlington Rd
Bloomington, IN 47404


Specialties & Details Slice


Pediatrics, Medical & Molecular Genetics

Conditions & Treatments:

Alpha-1 Antitrypsin Deficiency Gene Test, Ashkenazi Jewish Genetic Panel, Cardiovascular Genetics, Cardiovascular Genetics Program, Clinical Genetics, Cystic Fibrosis Program, Cystic Fibrosis Testing, Down Syndrome Screening, Dysmorphology, Genetic Counseling, Genetic Testing, Genetic Testing and Screening, Newborn Screening, Syndromology, Tay-Sachs Test, Teratogen Consultation, ASA, Atrial Septal Defect, Atrioventricular Septal Defect, Autosomal Recessive Disease, Bicuspid Aortic Valve, Birth Defects, Bone Dysplasia, Carnitine Deficiency, Chromosomal Abnormalities, Coarctation of the Aorta, Congenital Heart Defects, Congenital Heart Disease, Connective Tissue Disorders, Cystic Fibrosis, Developmental Delay, Disorders of Sexual Development, Down Syndrome, Fabry, Fatty Acid Oxidation Disorders, Fetal Alcohol Spectrum Disorders, Galactosemia, Gaucher, Genetic Conditions, Genetic Heart Disease, Glutaric Acidemia, Glycogen Storage Diseases, Homocystinuria, Hunter Syndrome, Hurler Syndrome, Hypertrophic Cardiomyopathy, Inborn Metabolism Errors, Inherited Disorders, Klinefelter Syndrome, LCHAD, Maroteaux Lamy Syndrome, MCAD, Metabolism Disorders, Mitochondrial Disorders, MPS, Patent Foramen Ovale, Phenylketonuria, Pompe, PPA, Pulmonary Valve Stenosis, SCAD, Sickle Cell Trait, Sly Syndrome, Tay-Sachs Disease, Tetralogy of Fallot, Thalassemia, Tricuspid Atresia, Turner Syndrome, Tyrosinemia, Urea Cycle Disorders, Vascular Ehlers-Danlos Syndrome, Ventricular Septal Defect, VLCAD, Carbamoyl Phosphate Synthetase Deficiency, Amino Acidopathies, Hyperammonemia, Autism, Intellectual Disability, Cleft Palate, Digeorge Syndrome, Patau Syndrome (Trisomy 13), Edwards Syndrome (Trisomy 18), Congenital Hearing Loss, Beckwith-Wiedmann Syndrome, Russell-Silver Syndrome, Chromosomal Deletions, Chromosomal Duplications, Angelman Syndrome


School of Medicine:

Indiana University School of Medicine


Indiana University School of Medicine - Pediatrics


Indiana University School of Medicine - Pediatrics


Indiana University School of Medicine - Medical Genetics

Hospitals & Affiliations

Hospital Privileges:

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

Physician Group:

IU Health Physicians, Riley Physicians


Research Publications
* Information provided by PubMed