Overview
Tarachandra Narumanchi is a Medical Genetics specialist and a Pediatrics provider in Oklahoma City, Oklahoma. Dr. Narumanchi and is rated as an Experienced provider by MediFind in the treatment of Vascular Ehlers-Danlos Syndrome (VEDS). His top areas of expertise are Phenylketonuria (PKU), Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Tyrosinemia Type 2.
His clinical research consists of co-authoring 2 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years.
Insurance
Please contact the provider to confirm they accept your insurance or if you don't see your insurance listed.
Accepted insurance plans
- Cigna
- Blue Cross Blue Shield
- Anthem
- CareSource
- Humana
Locations
1200 Childrens Ave, Oklahoma City, OK 73104
Additional Areas of Focus
Dr. Narumanchi has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
1 Clinical Trials
Areas of Expertise
When evaluating expertise, MediFind pulls from factors such as the number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
To learn more about how MediFind determines the expertise levels, check out our expert tiers page.
- Advanced
- Chromosome 10q Deletion
- Citrullinemia
- Dihydropteridine Reductase Deficiency
- Maternal Hyperphenylalaninemia
- Phenylketonuria (PKU)
- Tyrosinemia Type 1
- Experienced
- Brittle Cornea Syndrome
- Dandy-Walker Syndrome
- Ehlers-Danlos Syndrome (EDS)
- Gerstmann-Straussler-Scheinker Syndrome
- Glutaric Acidemia Type 1
- Hyperlysinemia