Overview
Giao Quach is a primary care provider, practicing in Family Medicine in Phoenix, Arizona. Dr. Quach is rated as an Experienced provider by MediFind in the treatment of Peripheral Artery Disease. His top areas of expertise are Type 2 Diabetes (T2D), Diabetic Neuropathy, Protein S Deficiency, and Congenital Antithrombin 3 Deficiency.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- MEDICARE MAPD
- MEDICARE SNP
- OTHER MEDICARE
- OTHER MEDICARE PART D
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- PPO
- MEDICARE MAPD
- OTHER MEDICARE
Accepted plan types not found. Please verify directly with the provider.
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MANAGED MEDICAID
- OTHER MEDICAID
- STATE MEDICAID
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- EPO
- HMO
- HMO
- EPO
- HMO
- POS
- PPO
- MEDICARE DISCOUNT CARD
- MEDICARE PDP
- OTHER MEDICARE
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
3137 W Indian School Rd, Phoenix, AZ 85017
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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
- Experienced
- Alzheimer's DiseaseDr. Quach isExperienced. Learn about Alzheimer's Disease.
- Apparent Mineralocorticoid ExcessDr. Quach isExperienced. Learn about Apparent Mineralocorticoid Excess.
- BullaeDr. Quach isExperienced. Learn about Bullae.
- Cerebellar DegenerationDr. Quach isExperienced. Learn about Cerebellar Degeneration.
- Chronic Obstructive Pulmonary Disease (COPD)
- Congenital Antithrombin 3 DeficiencyDr. Quach isExperienced. Learn about Congenital Antithrombin 3 Deficiency.