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 Mitochondrial Complex 1 Deficiency. 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
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider in Palo Alto, California. Dr. Enns is rated as an Elite provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. His top areas of expertise are Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Cholesteryl Ester Storage Disease, and Arginase Deficiency. Dr. Enns is currently accepting new patients.
Joseph Shieh is a Medical Genetics specialist and a Pediatrics provider in San Francisco, California. Dr. Shieh is rated as an Advanced provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. His top areas of expertise are Neurofibromatosis Type 1 (NF1), Myhre Syndrome, Neurofibromatosis, and Clouston Syndrome.
Ucsf Medical Group Business Services
Jeffrey Ralph is a Neurologist and a Pediatrics provider in San Francisco, California. Dr. Ralph is rated as a Distinguished provider by MediFind in the treatment of Mitochondrial Complex 1 Deficiency. His top areas of expertise are Peripheral Neuropathy, Miller-Fisher Syndrome, Chronic Polyradiculoneuritis, and Guillain-Barre Syndrome.
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.