Melissa D. Lah, MD
Pediatrics | Medical & Molecular Genetics
4.8 out of 5 stars
Score is an average of all responses to care provider related questions on our nationally-recognized NRC Health Patient Experience Survey.
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Accepting New Patients (Referral Required)
- Biography
- Insurance
- Locations
- Specialties & Details
- Ratings & Reviews
Biography
Dr. Melissa D. Lah specializes in Medical Genetics for Riley Medical & Molecular Genetics. Dr. Lah earned her medical degree at Indiana University School of Medicine. She then completed an internship and residency at Indiana University School of Medicine - Pediatrics and a fellowship at Indiana University School of Medicine - Medical Genetics.
Dr. Lah currently has a rating of 4.8 stars out of 5 with over 50 ratings. In a recent five-star review, a patient remarked: "It was very fast and efficient and she was through and nice."
Dr. Lah's primary location is Riley Medical & Molecular Genetics, 1002 Wishard Blvd, Indianapolis, IN 46202. She also sees patients at an office in Bloomington.
Insurance
Insurance plans accepted by this provider are below.
- Aetna Medicare Advantage
- Anthem Blue Cross Blue Shield
- Anthem Healthy Indiana Plan
- Anthem Hoosier Care Connect
- Anthem Hoosier Healthwise
- Anthem Medicare Advantage
- Anthem Medicare HMO
- Anthem Medicare PPO
- Anthem Pathway Essentials Network
- Care Source Healthy Indiana Plan
- Care Source Hoosier Healthwise
Cigna
Cofinity
Community Health Alliance
- Community Health Network - Employee Plan
- ProHealth/Community Health System
- CorVel/Corecare - Workers Compensation
Coventry/First Health
Deaconess OneCare
- Encore Workers Compensation
EyeMed
- Health Alliance Medicare Advantage
- Humana Medicare Advantage
- Indiana Health Network - Workers Compensation
- Indiana University Health - Workers Compensation
- IU Health Plans Medicare Advantage
Lutheran Preferred
- Managed Health Services Healthy Indiana Plan
- Managed Health Services Hoosier Care Connect
- Managed Health Services Hoosier Healthwise
- Managed Health Services Medicare Advantage
- MDWise Excel Healthy Indiana Plan
- MDWise Excel Hoosier Healthwise
MultiPlan/PHCS
NaphCare
- Parkview Health Plan Signature Care PPO
- Point Comfort - Refugee Medical Assistance Program
- Point Comfort - Unaccompanied Children Program
Sagamore
Select Health Network
SIHO
Spectera
Suburban Health Organization
- The Healthcare Group Encircle
- The Healthcare Group Encore
- TriCare Select
- United DSNP
- United HMO
- United HealthCare
- United HealthCare Hoosier Care Connect
- United Medicare Advantage
- United PPO
- VA - CCN via United Healthcare
Vision Service Plan (VSP)
Note: Although this listing was accurate at the time of posting, insurances change regularly, and insurance plans listed may not be accepted at all office locations for this provider. Please confirm with your insurance company that this provider is covered by your plan before your appointment.
Locations
Specialties & Details
Specialties:
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-Wiedemann Syndrome, Russell-Silver Syndrome, Chromosomal Deletions, Chromosomal Duplications, Angelman Syndrome
Education
School of Medicine:
Indiana University School of Medicine
Internship:
Indiana University School of Medicine - Pediatrics
Residency:
Indiana University School of Medicine - Pediatrics
Fellowship:
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
Research Publications
* Information provided by PubMed