The 20 Best Ornithine Translocase Deficiency Doctors in The United States

Markey Mcnutt is an Internal Medicine specialist and an Endocrinologist practicing medicine in Dallas, Texas. Dr. Mcnutt is rated as a Distinguished provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 122 other conditions, according to our data. His clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Phenylketonuria (PKU), and Multiple Sulfatase Deficiency.

Gerard Murphy is a primary care provider, practicing in Family Medicine in Chilhowie, Virginia. Dr. Murphy is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 25 other conditions, according to our data. His clinical expertise encompasses Familial Hypertension, Maturity Onset Diabetes of the Young, Glucocorticoid-Remediable Aldosteronism, and Hypertension. Dr. Murphy is board certified in  .

Philip Baney is a primary care provider, practicing in Family Medicine in Hamburg, Pennsylvania. Dr. Baney is rated as an Experienced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 8 other conditions, according to our data. His clinical expertise encompasses Maturity Onset Diabetes of the Young, High Cholesterol, Type 2 Diabetes (T2D), and Familial Hypertension. Dr. Baney is board certified in American Board Of Family Medicine.

Dr. Ada Hamosh is the Dr. Frank V. Sutland Professor of Pediatric Genetics in the Departments of Genetic Medicine and Pediatrics. Since 2002, she has served as clinical director of the McKusick-Nathans Institute of Genetic Medicine, now Department of Genetic Medicine and scientific director of the Online Mendelian Inheritance in Man® (OMIM), a catalog of more than 16,800 human genes and genetic disorders created by Dr. Victor A. McKusick. Her research centers the molecular basis of Mendelian disorders, the integration of genetics into clinical practice and the diagnosis and management of inborn errors of metabolism. Dr. Hamosh earned a bachelor’s degree in biology from Wesleyan University, a medical degree from Georgetown University School of Medicine and a master’s of public health from Johns Hopkins University School of Public Health. She later completed a fellowship in medical and biochemical genetics from the Johns Hopkins School of Medicine, before joining the Johns Hopkins faculty in 1992. Dr. Hamosh began her genetics career focusing on cystic fibrosis, serving as coordinator of the International Cystic Fibrosis Genotype-Phenotype Consortium. She served as chair of the Maryland State Advisory Council for Hereditary & Congenital Disorders from 2001-2009, during which time she also served on the executive committee of the Genetic Counseling Training Program, run by Johns Hopkins University and the National Human Genome Research Institute. Dr. Hamosh has authored more than 128 publications on a variety of topics. In addition, she is a member of 16 professional associations and advisory committees including the American Society of Human Genetics, the Steering Committee of the Global Alliance for Genomics and Health, and the executive board of the Human Genome Organization, of which she will be President from 2023-2025. Dr. Hamosh was recognized in Baltimore magazine as one of the region’s top doctors in 2013, and 2016-2020. Dr. Hamosh is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 27 other conditions, according to our data. Her clinical expertise encompasses Methylmalonic Acidemia, Maple Syrup Urine Disease, Ornithine Transcarbamylase Deficiency, Phenylketonuria (PKU), and Deep Brain Stimulation. Dr. Hamosh is board certified in American Board Of Medical Genetics And Genomics.

Meral Gunay-Aygun is a professor of pediatrics and genetic medicine at Johns Hopkins University School of Medicine. Dr. Gunay-Aygun specializes in the diagnosis and treatment of children and adults with inherited metabolic diseases including diagnostic evaluation and follow-up of newborns with abnormal newborn screens for inherited metabolic diseases. After serving 14 years as an attending physician at The Johns Hopkins Hospital in Baltimore, she joined the medical staff of Johns Hopkins All Children’s Hospital in St. Petersburg, Florida in 2022. Dr. Gunay-Aygun earned her medical degree from Hacettepe University School of Medicine, Ankara, Turkey. She completed pediatrics and medical genetics residencies at Case Western Reserve University, Cleveland, Ohio, and a biochemical genetics fellowship at the National Institutes of Health’s National Human Genome Research Institute, Bethesda, Maryland. She has made numerous research contributions, especially in the study of inherited ciliopathies, for which she has earned international recognition. Dr. Gunay-Aygun received the Innovative Leadership Award from Genetic Alliance, as well as the NHGRI Merit Award for her research on Autosomal Recessive Polycystic Kidney Disease/Congenital Hepatic Fibrosis. She is a member of myriad professional organizations, including the American Society of Human Genetics, the American Academy of Pediatrics, the Society of Pediatric Research and the Society for Inherited Metabolic Disorders. Dr. Gunay is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 7 other conditions, according to our data. Her clinical expertise encompasses Phenylketonuria (PKU), Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, and Argininosuccinic Aciduria. Dr. Gunay is board certified in American Board Of Medical Genetics And Genomics and American Board Of Pediatrics.

Jessica Priestley is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Grand Rapids, Michigan. She has been practicing medicine for over 8 years. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 21 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Biotinidase Deficiency, Ornithine Transcarbamylase Deficiency, and Multiple Sulfatase Deficiency. Dr. Priestley is board certified in American Board Of Medical Genetics And Genomics, American Board Of Medical Genetics And Genomics, and American Board Of Pediatrics.

Mari Mori is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Orlando, Florida. Dr. Mori is rated as an Experienced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 5 other conditions, according to our data. Her clinical expertise encompasses FG Syndrome, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Von Gierke Disease, and Ornithine Transcarbamylase Deficiency. Dr. Mori is currently accepting new patients.

Darren Gibson is a primary care provider, practicing in Emergency Medicine in Abingdon, Virginia. Dr. Gibson is rated as an Experienced provider by MediFind in the treatment of Ornithine Translocase Deficiency. His clinical expertise encompasses Acute Cystitis, Morning Sickness, Hospital-Acquired Pneumonia, and Atypical Pneumonia. Dr. Gibson is board certified in American Board Of Family Medicine.

Darrel Waggoner is a Medical Genetics provider practicing medicine in Chicago, Illinois. Dr. Waggoner is rated as a Distinguished provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 5 other conditions, according to our data. His clinical expertise encompasses Ornithine Transcarbamylase Deficiency, Ornithine Translocase Deficiency, Kabuki Syndrome, Caudal Appendage Deafness, and Gastrostomy. Dr. Waggoner is currently accepting new patients.

Marshall Summar is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Chevy Chase, Maryland. Dr. Summar is rated as a Distinguished provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 7 other conditions, according to our data. His clinical expertise encompasses Argininosuccinic Aciduria, Urea Cycle Disorders (UCD), Propionic Acidemia, and Ornithine Translocase Deficiency.

David Sweetser is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Sweetser is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Hypotonia, Ornithine Translocase Deficiency, Ornithine Transcarbamylase Deficiency, and Propionic Acidemia. Dr. Sweetser is board certified in Pediatrics, Clinical Biochemical Genetics, Pediatric Hematology-Oncology, and Clinical Genetics And Genomics.

Richard Chang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chang is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 155 other conditions, according to our data. His clinical expertise encompasses Citrullinemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Adrenoleukodystrophy (ALD). Dr. Chang is currently accepting new patients.

Amy Kritzer is a Pediatrics provider practicing medicine in Boston, Massachusetts. Dr. Kritzer is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 33 other conditions, according to our data. Her clinical expertise encompasses Maternal Hyperphenylalaninemia, Phenylketonuria (PKU), Biotinidase Deficiency, and Smith-Lemli-Opitz Syndrome. Dr. Kritzer is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics And Genomics.

Jose Abdenur is a Medical Genetics provider practicing medicine in Orange, California. Dr. Abdenur is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 41 other conditions, according to our data. His clinical expertise encompasses Glycogen Storage Disease Type 9, Von Gierke Disease, Glycogen Storage Disease Type 3, and Malonyl-CoA Decarboxylase Deficiency. Dr. Abdenur is currently accepting new patients.

Madelena Martin is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Sacramento, California. Dr. Martin is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 12 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Phenylketonuria (PKU), and Fabry Disease. Dr. Martin is board certified in Medical Genetics And Genomics Clin Biochemical Genetic and Medical Genetics And Genomics Clin Genetics & Genomic. Dr. Martin is currently accepting new patients.

Carolyn Jones is a Medical Genetics provider practicing medicine in Winfield, Illinois. She has been practicing medicine for over 35 years. Dr. Jones is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. She is also highly rated in 101 other conditions, according to our data. Her clinical expertise encompasses Fabry Disease, Multiple Sulfatase Deficiency, Megalencephalic Leukoencephalopathy with Subcortical Cysts, and Danon Disease. Dr. Jones is board certified in American Board Of Medical Genetics And Genomics - Clinical Genetics And Genomics (Certified).

Raymond Wang is a Medical Genetics provider practicing medicine in Orange, California. Dr. Wang is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 46 other conditions, according to our data. His clinical expertise encompasses Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome), Mucopolysaccharidosis Type 4A (MPS IVA, Morquio Syndrome Type A), Mucopolysaccharidoses (MPS), and Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome).

Luis Umana is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Umana is rated as an Advanced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 177 other conditions, according to our data. His clinical expertise encompasses Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Classic Galactosemia, Biotinidase Deficiency, and 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency.

Michael Carroll is a primary care provider, practicing in Family Medicine and Obstetrics and Gynecology in Traverse City, Michigan. He has been practicing medicine for over 30 years. Dr. Carroll is rated as an Experienced provider by MediFind in the treatment of Ornithine Translocase Deficiency. He is also highly rated in 45 other conditions, according to our data. His clinical expertise encompasses Type 2 Diabetes (T2D), Maturity Onset Diabetes of the Young, Hypertension, and Familial Hypertension. Dr. Carroll is board certified in American Board Of Family Medicine, Family Medicine - 1999. Dr. Carroll is currently accepting new patients.

To provide our patients with compassionate quality medical care. Dr. Patel is rated as an Experienced provider by MediFind in the treatment of Ornithine Translocase Deficiency. Her clinical expertise encompasses Sepsis, Leukocytosis, Peptic Ulcer, and Necrosis. Dr. Patel is board certified in Internal Medicine and Internal Medicine (Sub: Hospice And Palliative Medici. Dr. Patel is currently accepting new patients.