Overview
Renata Gallagher is a Medical Genetics specialist and a Pediatrics provider in San Francisco, California. Dr. Gallagher is rated as an Advanced provider by MediFind in the treatment of Gaucher Disease Type 1. Her top areas of expertise are Gaucher Disease Type 3, Gaucher Disease Type 1, Gaucher Disease Type 2, and Gaucher Disease.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- HMO
- INDEMNITY
- POS
- PPO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- HMO
- POS
- PPO
Locations
Seymour Packman is a Medical Genetics provider in San Francisco, California. Dr. Packman is rated as a Distinguished provider by MediFind in the treatment of Gaucher Disease Type 1. His top areas of expertise are Gaucher Disease Type 1, Gaucher Disease, Fabry Disease, and Fucosidosis.
Lpch Medical Group Div Of Lucile
Chung Lee is a Medical Genetics specialist and a Pediatrics provider in Palo Alto, California. Dr. Lee has been practicing medicine for over 18 years and is rated as an Advanced provider by MediFind in the treatment of Gaucher Disease Type 1. Her top areas of expertise are Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Maple Syrup Urine Disease, and Carnitine Palmitoyltransferase 2 Deficiency.
Bryce Mendelsohn is a Medical Genetics provider in Oakland, California. Dr. Mendelsohn is rated as an Advanced provider by MediFind in the treatment of Gaucher Disease Type 1. His top areas of expertise are Chromosome 10q Deletion, Chromosome 13q Duplication, Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency.
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
- Advanced
- Acid Sphingomyelinase Deficiency (ASMD)Dr. Gallagher isAdvanced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- AlkaptonuriaDr. Gallagher isAdvanced. Learn about Alkaptonuria.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Coenzyme Q Cytochrome C Reductase Deficiency
- Fabry DiseaseDr. Gallagher isAdvanced. Learn about Fabry Disease.
- Experienced
- Danon DiseaseDr. Gallagher isExperienced. Learn about Danon Disease.
- Dihydropteridine Reductase DeficiencyDr. Gallagher isExperienced. Learn about Dihydropteridine Reductase Deficiency.
- Glutaric Acidemia Type 2Dr. Gallagher isExperienced. Learn about Glutaric Acidemia Type 2.
- Inborn Amino Acid Metabolism DisorderDr. Gallagher isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Maple Syrup Urine DiseaseDr. Gallagher isExperienced. Learn about Maple Syrup Urine Disease.
- Maternal HyperphenylalaninemiaDr. Gallagher isExperienced. Learn about Maternal Hyperphenylalaninemia.