Overview
Janet Thomas is a Medical Genetics specialist and a Pediatrics provider in Aurora, Colorado. Dr. Thomas is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Phenylketonuria (PKU), Homocystinuria, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- POS
- PPO
- EPO
- INSURANCE PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER COMMERCIAL
- OTHER MEDICARE
- PPO
- EPO
- HMO
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- OTHER MEDICARE
- POS
- PPO
- EPO
- HMO
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- OTHER COMMERCIAL
- POS
- PPO
- EPO
- HMO
- POS
- PPO
Locations
13123 E 16th Ave, Aurora, CO 80045
Additional Areas of Focus
Dr. Thomas 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.
Kathryn Kronquist is a Medical Genetics provider in Aurora, Colorado. Dr. Kronquist is rated as a Distinguished provider by MediFind in the treatment of Homocystinuria. Her top areas of expertise are Glycine Encephalopathy, Micrognathia, and Homocystinuria.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as 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.
Learn more about MediFind’s expert tiers
- Elite
- Phenylketonuria (PKU)Dr. Thomas isElite. Learn about Phenylketonuria (PKU).
- Distinguished
- HomocystinuriaDr. Thomas isDistinguished. Learn about Homocystinuria.
- Advanced
- Dihydropteridine Reductase Deficiency
- Galactose Epimerase DeficiencyDr. Thomas isAdvanced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaDr. Thomas isAdvanced. Learn about Galactosemia.
- Maternal HyperphenylalaninemiaDr. Thomas isAdvanced. Learn about Maternal Hyperphenylalaninemia.
- Tyrosinemia Type 1Dr. Thomas isAdvanced. Learn about Tyrosinemia Type 1.
- Tyrosinemia Type 2Dr. Thomas isAdvanced. Learn about Tyrosinemia Type 2.
- Experienced
- Classic GalactosemiaDr. Thomas isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyDr. Thomas isExperienced. Learn about Galactokinase Deficiency.
- Mucopolysaccharidoses (MPS)Dr. Thomas isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency