Overview
Pamela Moore is a Pediatrics specialist and a Hospital Medicine provider in University Place, Washington. Her top areas of expertise are Glycogen Storage Disease Type 7, Glycogen Storage Disease Type 13, Glycogen Storage Disease Type 0, and Phosphoglycerate Mutase Deficiency. Dr. Moore is currently accepting new patients.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- MANAGED MEDICAID PLAN
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE PART D
- PPO
- EPO
- PPO
- HMO
- POS
- EPO
- HMO
- POS
- PPO
Locations
The Association Of University Physicians
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Office
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Ghayda Mirzaa is a Medical Genetics specialist and a Pediatrics provider in Seattle, Washington. Dr. Mirzaa is highly rated in 19 conditions, according to our data. Her top areas of expertise are Increased Head Circumference, Cortical Dysplasia, Achalasia Microcephaly Syndrome, and Microcephaly. Dr. Mirzaa is currently accepting new patients.
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
- Glycogen Storage Disease Type 0Dr. Moore isExperienced. Learn about Glycogen Storage Disease Type 0.
- Glycogen Storage Disease Type 13Dr. Moore isExperienced. Learn about Glycogen Storage Disease Type 13.
- Glycogen Storage Disease Type 7Dr. Moore isExperienced. Learn about Glycogen Storage Disease Type 7.
- Glycogen Storage Disease Type 9Dr. Moore isExperienced. Learn about Glycogen Storage Disease Type 9.
- Phosphoglycerate Kinase DeficiencyDr. Moore isExperienced. Learn about Phosphoglycerate Kinase Deficiency.
- Phosphoglycerate Mutase DeficiencyDr. Moore isExperienced. Learn about Phosphoglycerate Mutase Deficiency.