Overview
Renata Gallagher is a Medical Genetics specialist and a Pediatrics provider in San Francisco, California. Dr. Gallagher is rated as an Experienced provider by MediFind in the treatment of Progressive External Ophthalmoplegia. Her top areas of expertise are Gaucher Disease Type 2, Gaucher Disease Type 1, Gaucher Disease Type 3, 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 Pediatrics specialist and a Medical Genetics provider in Palo Alto, California. Dr. Enns is rated as an Elite provider by MediFind in the treatment of Progressive External Ophthalmoplegia. His top areas of expertise are Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Cholesteryl Ester Storage Disease. Dr. Enns is currently accepting new patients.
Alicia Aycinena is a Medical Genetics provider in San Francisco, California. Dr. Aycinena is rated as an Advanced provider by MediFind in the treatment of Progressive External Ophthalmoplegia. Her top areas of expertise are Sjogren-Larsson Syndrome, Kearns-Sayre Syndrome, Retinopathy Pigmentary Mental Retardation, and Bardet-Biedl Syndrome.
Lpch Medical Group Div Of Lucile
Christina Tise is a Medical Genetics provider in Palo Alto, California. Dr. Tise is rated as an Advanced provider by MediFind in the treatment of Progressive External Ophthalmoplegia. Her top areas of expertise are Zellweger Syndrome, 2q37 Deletion Syndrome, Urea Cycle Disorders (UCD), and Adrenoleukodystrophy (ALD).
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.