The 20 Best Citrullinemia Doctors in The United States
Find the Top Citrullinemia Experts and Specialists
St. Christopher's Pediatric Associates Genetics - E. Erie Avenue
Tarachandra Narumanchi is a Medical Genetics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Narumanchi is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. He is also highly rated in 21 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Phenylketonuria (PKU), Maternal Hyperphenylalaninemia, and Dihydropteridine Reductase Deficiency. Dr. Narumanchi is board certified in American Board Of Medical Genetics And Genomics.
Rubenstein Child Health Building
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 Citrullinemia. 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.
Florida Hospital Medical Group Inc
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 Citrullinemia. 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.
Children's National Hospital
Andrea Gropman is a Pediatrics provider practicing medicine in Washington, Washington, D.c.. Dr. Gropman is rated as a Distinguished provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 37 other conditions, according to our data. Her clinical expertise encompasses Klinefelter Syndrome, Urea Cycle Disorders (UCD), MELAS Syndrome, Ornithine Transcarbamylase Deficiency, and Hormone Replacement Therapy (HRT).
Childrens Health Care Associates Inc
Can Ficicioglu is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Philadelphia, Pennsylvania. Dr. Ficicioglu is rated as a Distinguished provider by MediFind in the treatment of Citrullinemia. He is also highly rated in 51 other conditions, according to our data. His clinical expertise encompasses Classic Galactosemia, Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome), Urea Cycle Disorders (UCD), and Gaucher Disease.
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 Citrullinemia. 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.
UT Southwestern - Pediatrics
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 Citrullinemia. 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.
UT Southwestern - Pediatric Genetics
Laura Mackay is a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Mackay is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 132 other conditions, according to our data. Her clinical expertise encompasses Isovaleric Acidemia, Beta-Ketothiolase Deficiency, Biotinidase Deficiency, and Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency.
UT Southwestern - Internal Medicine Subspecialties
Markey Mcnutt is an Internal Medicine specialist and an Endocrinologist practicing medicine in Dallas, Texas. Dr. Mcnutt is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. 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.
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 Citrullinemia. 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).
UT Southwestern - Pediatrics
Garrett Gotway is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Dallas, Texas. Dr. Gotway is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. He is also highly rated in 131 other conditions, according to our data. His clinical expertise encompasses Yunis-Varon Syndrome, Grix Blankenship Peterson Syndrome, Mckusick-Kaufman Syndrome, and Blepharocheilodontic Syndrome.
Corewell Health Grand Rapids Hospitals Biochemical Genetics - 25 Michigan St NE
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 Experienced provider by MediFind in the treatment of Citrullinemia. 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.
C. S. Mott Children's Hospital
Dr. Pritchard is a Michigan native who returned to the University of Michigan to join the faculty here in 2019 after completing her pediatrics and genetics residencies and biochemical genetics fellowship. She enjoys care of complex patients with rare genetic diseases. Dr. Pritchard is active in medical education as Program Director for the Medical Biochemical Genetics Fellowship program and Associate Program Director for the Medical Genetics and Genomics training programs.Outside of work, Dr. Pritchard enjoys cooking, reading, hiking, and spending time with her husband and two daughters. Dr. Pritchard is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 149 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Cockayne Syndrome Type 2.
University Of Vermont Medical Center Inc
Katherine Anderson is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Burlington, Vermont. Dr. Anderson is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Ring Chromosome 14, Dihydropteridine Reductase Deficiency, Maternal Hyperphenylalaninemia, and Phenylketonuria (PKU). Dr. Anderson is currently accepting new patients.
Cristel Chapel is a Medical Genetics provider practicing medicine in Orange, California. Dr. Chapel is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Batten Disease, CLN4 Disease, CLN2 Disease, and CLN3 Disease. Dr. Chapel is currently accepting new patients.
Jose Abdenur is a Medical Genetics provider practicing medicine in Orange, California. Dr. Abdenur is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. 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.
UT Southwestern - Pediatric Genetics
Angela Scheuerle is a Pediatrics specialist and a Medical Genetics provider practicing medicine in Dallas, Texas. Dr. Scheuerle is rated as an Experienced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 172 other conditions, according to our data. Her clinical expertise encompasses Hennekam Syndrome, Fetal Akinesia Sequence, Hemihyperplasia, and Incontinentia Pigmenti.
Baylor College Of Medicine
William Craigen is a Pediatrics provider practicing medicine in Houston, Texas. Dr. Craigen is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. He is also highly rated in 12 other conditions, according to our data. His clinical expertise encompasses MELAS Syndrome, Citrullinemia, Mitochondrial Complex 1 Deficiency, and Propionic Acidemia.
Mount Sinai School Of Medicine
Jaya Ganesh is a Pediatrics provider practicing medicine in New York, New York. Dr. Ganesh is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. She is also highly rated in 64 other conditions, according to our data. Her clinical expertise encompasses Acid Sphingomyelinase Deficiency (ASMD), Niemann-Pick Disease, Pompe Disease, and Danon Disease.
Ann & Robert H. Lurie Children's Hospital Of Chicago
Joshua Baker is a Pediatrics provider practicing medicine in Chicago, Illinois. Dr. Baker is rated as an Advanced provider by MediFind in the treatment of Citrullinemia. He is also highly rated in 152 other conditions, according to our data. His clinical expertise encompasses Urea Cycle Disorders (UCD), Ornithine Transcarbamylase Deficiency, Acid Sphingomyelinase Deficiency (ASMD), and Propionic Acidemia.
Last Updated: 06/30/2026


