Overview
Renata Gallagher is a Medical Genetics specialist and a Pediatrics provider practicing medicine in San Francisco, California.
Dr. Gallagher is highly rated in 19 conditions, according to our data. Her clinical expertise encompasses Gaucher Disease Type 3, Gaucher Disease Type 1, Gaucher Disease Type 2, and Gaucher Disease.
Specialties
Licenses
Languages Spoken
Gender
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
David Stevenson is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Stevenson is highly rated in 100 conditions, according to our data. His clinical expertise encompasses Neurofibromatosis Type 1 (NF1), Neurofibromatosis, RASopathies, Costello Syndrome, and Deep Brain Stimulation.
Lpch Medical Group Div Of Lucile
Gregory Enns is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Palo Alto, California. Dr. Enns is highly rated in 54 conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Methylmalonic Acidemia, Arginase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency. Dr. Enns is currently accepting new patients.
Center For Complex Obstetric Medicine
Dr. Mary E. Norton is a perinatologist and clinical geneticist who cares for pregnant patients who have a fetus with a birth defect or genetic disorder or are at risk for such a condition. She performs obstetric ultrasounds, counsels patients with abnormal ultrasounds and performs prenatal tests like amniocentesis and chorionic villus sampling. She also interprets complex genetic tests, especially when abnormalities are found. Norton's areas of interest in research include applying new genetic tests to prenatal diagnosis and fetal disease, as well as patient decision-making around genetic testing and obstetrical ultrasound. She is co-director of the Center for Maternal-Fetal Precision Medicine at UCSF, as well as the David E. Thorburn, M.D. and Kate McKee Thorburn Endowed Chair in Perinatal Medicine and Genetics at UCSF. Norton earned her medical degree at the University of Washington. She completed a residency in obstetrics and gynecology at Tufts University followed by a fellowship in maternal-fetal medicine and clinical genetics at UCSF. After several years at Brigham and Women's Hospital and Harvard Medical School, she returned to San Francisco and joined UCSF Medical Center in 1998. Dr. Norton is highly rated in 20 conditions, according to our data. Her clinical expertise encompasses Fetal Edema, Hydrops Fetalis, Alpha Thalassemia, and Hemolytic Disease of the Newborn. Dr. Norton is board certified in American Board Of Obstetrics And Gynecology, Obstetrics & Gynecology, American Board Of Medical Genetics And Genomics, Clinical Genetics And Genomics, and American Board Of Obstetrics And Gynecology, Maternal-Fetal Medicine. Dr. Norton is currently accepting new patients.
Frequently Asked Questions about Dr. Renata C. Gallagher
How do I make an appointment with Dr. Renata C. Gallagher?
You can book an appointment with Dr. Renata C. Gallagher by calling their office at 415-476-9997. MediFind provides direct contact information so you can schedule visits, second opinions, or consultations without navigating third-party calendars.
Is Dr. Renata C. Gallagher a top-rated expert for Gaucher Disease Type 3?
MediFind is an objective health platform that identifies experts based on real-world data. Dr. Renata C. Gallagher is classified as an Advanced expert for Gaucher Disease Type 3, 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. Renata C. Gallagher specialize in?
While Dr. Renata C. Gallagher is a Medical Genetics, they have specific expertise in Gaucher Disease Type 3, Gaucher Disease Type 1, and Gaucher Disease Type 2. MediFind analyzes a doctor's articles and referral patterns to identify their specific areas of focus within Medical Genetics.
Does Dr. Renata C. Gallagher accept my insurance?
Dr. Renata C. Gallagher accepts most major insurance plans, including Humana and Medicaid. We recommend calling the office directly at 415-476-9997 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
- 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.
- Gaucher DiseaseDr. Gallagher isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 1Dr. Gallagher isAdvanced. Learn about Gaucher Disease Type 1.
- Gaucher Disease Type 2Dr. Gallagher isAdvanced. Learn about Gaucher Disease Type 2.
- Gaucher Disease Type 3Dr. Gallagher isAdvanced. Learn about Gaucher Disease Type 3.
- Megalencephalic Leukoencephalopathy with Subcortical Cysts
- MELAS SyndromeDr. Gallagher isAdvanced. Learn about MELAS Syndrome.
- Mitochondrial Complex 1 DeficiencyDr. Gallagher isAdvanced. Learn about Mitochondrial Complex 1 Deficiency.
- Mitochondrial Trifunctional Protein Deficiency
- Multiple Sulfatase DeficiencyDr. Gallagher isAdvanced. Learn about Multiple Sulfatase Deficiency.
- Ornithine Transcarbamylase DeficiencyDr. Gallagher isAdvanced. Learn about Ornithine Transcarbamylase Deficiency.
- Ornithine Translocase DeficiencyDr. Gallagher isAdvanced. Learn about Ornithine Translocase Deficiency.
- Phenylketonuria (PKU)Dr. Gallagher isAdvanced. Learn about Phenylketonuria (PKU).
- Thymidine Kinase 2 Deficiency (TK2d)Dr. Gallagher isAdvanced. Learn about Thymidine Kinase 2 Deficiency (TK2d).
- 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.
- Niemann-Pick DiseaseDr. Gallagher isExperienced. Learn about Niemann-Pick Disease.
- Pompe DiseaseDr. Gallagher isExperienced. Learn about Pompe Disease.
- Progressive External OphthalmoplegiaDr. Gallagher isExperienced. Learn about Progressive External Ophthalmoplegia.
- ReticulohistiocytomaDr. Gallagher isExperienced. Learn about Reticulohistiocytoma.
- SplenomegalyDr. Gallagher isExperienced. Learn about Splenomegaly.
- Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency
