Overview
Annette Feigenbaum is a Medical Genetics provider practicing medicine in San Diego, California.
Dr. Feigenbaum is highly rated in 6 conditions, according to our data. Her clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Ornithine Transcarbamylase Deficiency, and Medium-Chain Acyl-CoA Dehydrogenase Deficiency.
She is actively involved in clinical research, co-authoring 50 peer reviewed articles.
Specialties
Licenses
Languages Spoken
Gender
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE-MEDICAID PLAN
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- OTHER COMMERCIAL
- OTHER MEDICARE
- OTHER MEDICARE PART D
- PPO
Accepted plan types not found. Please verify directly with the provider.
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
- EPO
- HMO
- INSURANCE PLAN
- MANAGED MEDICAID PLAN
- MEDICARE MAPD
- MEDICARE PDP
- MEDICARE SNP
- MEDICARE-MEDICAID PLAN
- OTHER MEDICARE
- OTHER MEDICARE PART D
Locations
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.
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Frequently Asked Questions about Dr. Annette S. Feigenbaum
How do I make an appointment with Dr. Annette S. Feigenbaum?
You can book an appointment with Dr. Annette S. Feigenbaum by calling their office at 858-576-1700. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Annette S. Feigenbaum a top-rated expert for Urea Cycle Disorders (UCD)?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Annette S. Feigenbaum is classified as an Distinguished expert for Urea Cycle Disorders (UCD), meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
What conditions does Dr. Annette S. Feigenbaum specialize in?
While Dr. Annette S. Feigenbaum is a Medical Genetics, they have specific expertise in Urea Cycle Disorders (UCD), Phenylketonuria (PKU), and Ornithine Transcarbamylase Deficiency. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Annette S. Feigenbaum participate in research or clinical trials?
Yes. Dr. Annette S. Feigenbaum has published 50 articles and abstracts on conditions like Urea Cycle Disorders (UCD). You can view a list of Dr. Annette S. Feigenbaum's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
Does Dr. Annette S. Feigenbaum accept my insurance?
Dr. Annette S. Feigenbaum accepts most major insurance plans, including Anthem BCBS and Blue Shield of California. We recommend calling the office directly at 858-576-1700 to verify that your specific plan is currently accepted before your visit.
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
- Distinguished
- Ornithine Transcarbamylase DeficiencyDr. Feigenbaum isDistinguished. Learn about Ornithine Transcarbamylase Deficiency.
- Phenylketonuria (PKU)Dr. Feigenbaum isDistinguished. Learn about Phenylketonuria (PKU).
- Urea Cycle Disorders (UCD)Dr. Feigenbaum isDistinguished. Learn about Urea Cycle Disorders (UCD).
- Advanced
- HomocystinuriaDr. Feigenbaum isAdvanced. Learn about Homocystinuria.
- Medium-Chain Acyl-CoA Dehydrogenase Deficiency
- Singleton-Merten SyndromeDr. Feigenbaum isAdvanced. Learn about Singleton-Merten Syndrome.
- Experienced
- Adrenoleukodystrophy (ALD)Dr. Feigenbaum isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Arginase DeficiencyDr. Feigenbaum isExperienced. Learn about Arginase Deficiency.
- Brachydactyly Mononen TypeDr. Feigenbaum isExperienced. Learn about Brachydactyly Mononen Type.
- Danon DiseaseDr. Feigenbaum isExperienced. Learn about Danon Disease.
- Dihydrolipoamide Dehydrogenase DeficiencyDr. Feigenbaum isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Dihydropteridine Reductase DeficiencyDr. Feigenbaum isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Fabry DiseaseDr. Feigenbaum isExperienced. Learn about Fabry Disease.
- Gaucher DiseaseDr. Feigenbaum isExperienced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Feigenbaum isExperienced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Feigenbaum isExperienced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Feigenbaum isExperienced. Learn about Gaucher Disease Type 3.
- HypermethioninemiaDr. Feigenbaum isExperienced. Learn about Hypermethioninemia.
- Inborn Amino Acid Metabolism DisorderDr. Feigenbaum isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Leigh SyndromeDr. Feigenbaum isExperienced. Learn about Leigh Syndrome.
- Maple Syrup Urine DiseaseDr. Feigenbaum isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Feigenbaum isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- Molybdenum Cofactor Deficiency (MoCD)Dr. Feigenbaum isExperienced. Learn about Molybdenum Cofactor Deficiency (MoCD).
- Mucopolysaccharidoses (MPS)Dr. Feigenbaum isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Multiple Sulfatase DeficiencyDr. Feigenbaum isExperienced. Learn about Multiple Sulfatase Deficiency.
- N-Acetyl-Alpha-D-Galactosaminidase Deficiency Type 3
- Newborn Low Blood SugarDr. Feigenbaum isExperienced. Learn about Newborn Low Blood Sugar.
- Ornithine Translocase DeficiencyDr. Feigenbaum isExperienced. Learn about Ornithine Translocase Deficiency.
- PGM1-CDGDr. Feigenbaum isExperienced. Learn about PGM1-CDG.
- Pompe DiseaseDr. Feigenbaum isExperienced. Learn about Pompe Disease.
- Propionic AcidemiaDr. Feigenbaum isExperienced. Learn about Propionic Acidemia.
- Pyruvate Decarboxylase DeficiencyDr. Feigenbaum isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyDr. Feigenbaum isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- SplenomegalyDr. Feigenbaum isExperienced. Learn about Splenomegaly.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency