The 20 Best Ornithine Transcarbamylase Deficiency Doctors Near Me in Michigan, US
Find the Top Ornithine Transcarbamylase Deficiency Experts and Specialists
C. S. Mott Children's Hospital
Ayesha Ahmad is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ahmad is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 45 other conditions, according to our data. Her clinical expertise encompasses Pompe Disease, Danon Disease, Von Gierke Disease, and Tyrosinemia Type 3. Dr. Ahmad is board certified in Clinical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Ahmad is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Shane Quinonez is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Quinonez is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 129 other conditions, according to our data. His clinical expertise encompasses Pompe Disease, Dihydrolipoamide Dehydrogenase Deficiency, MELAS Syndrome, and Maple Syrup Urine Disease. Dr. Quinonez is board certified in Pediatrics, American Board Of Pediatrics, Pediatrics - 2011, Clinical Biochemical Genetics, American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2015 , American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2024 , and Clinical Genetics & Genomics. Dr. Quinonez is currently accepting new patients.
Pediatric Otolaryngology Clinic
Kristen Lee is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 138 other conditions, according to our data. Her clinical expertise encompasses Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome. Dr. Lee is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics & Genomics. Dr. Lee is currently accepting new patients.
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. Dr. Priestley is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase 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 and American Board Of Pediatrics. Dr. Priestley is currently accepting new patients.
Pediatric Genetics Clinic
Elizabeth Ames is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Ames is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Delayed Growth, Noonan Syndrome, Cardiofaciocutaneous Syndrome, and Cardiomyopathic Lentiginosis. Dr. Ames is board certified in Pediatrics, Medical Biochemical Genetics, and Clinical Genetics & Genomics. Dr. Ames is currently accepting new patients.
Stacie Adams is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Grand Rapids, Michigan. Dr. Adams is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 20 other conditions, according to our data. Her clinical expertise encompasses Propionic Acidemia, Classic Galactosemia, Biotinidase Deficiency, and Galactosemia. Dr. Adams is currently accepting new patients.
C. S. Mott Children's Hospital
Christina Sloan-Heggen is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Sloan-Heggen is rated as an Advanced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 115 other conditions, according to our data. Her clinical expertise encompasses Chromosome 6q Duplication, Chromosome 8p Deletion, Delayed Growth, and Fragile XE Syndrome. Dr. Sloan-Heggen is board certified in Medical Biochemical Genetics and Clinical Genetics & Genomics. Dr. Sloan-Heggen is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Amanda Pritchard is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Pritchard is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 150 other conditions, according to our data. Her clinical expertise encompasses Microcephaly Deafness Syndrome, Propionic Acidemia, Delayed Growth, and Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant. Dr. Pritchard is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2019 , American Board Of Pediatrics, Pediatrics - 2016, and American Board Of Medical Genetics And Genomics, Medical Biochemical Genetics - 2019 . Dr. Pritchard is currently accepting new patients.
Pediatric Genetics Clinic
Tomoyasu Higashimoto is a Medical Genetics provider practicing medicine in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 110 other conditions, according to our data. His clinical expertise encompasses Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia. Dr. Higashimoto is board certified in Family Medicine and Clinical Genetics & Genomics. Dr. Higashimoto is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Mark Hannibal is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Hannibal is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 167 other conditions, according to our data. His clinical expertise encompasses Aase Syndrome, Alstrom Syndrome, Char Syndrome, and Filippi Syndrome. Dr. Hannibal is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2020 and Clinical Genetics & Genomics. Dr. Hannibal is currently accepting new patients.
University Of Michigan Pediatric Genetics Clinic
Catherine Keegan is a Medical Genetics specialist and a Pediatrics provider practicing medicine in Ann Arbor, Michigan. Dr. Keegan is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. She is also highly rated in 3 other conditions, according to our data. Her clinical expertise encompasses Intersex, Aarskog Syndrome, Turner Syndrome, and Hydrocephalus due to Congenital Stenosis of Aqueduct of Sylvius. Dr. Keegan is board certified in American Board Of Medical Genetics And Genomics, Clinical Biochemical Genetics - 2023. Dr. Keegan is currently accepting new patients.
East Michigan Hospitalists PLLC
Ponon Kumar is a primary care provider, practicing in Internal Medicine in Port Huron, Michigan. Dr. Kumar is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 47 other conditions, according to our data. His clinical expertise encompasses Necrosis, Hereditary Pancreatitis, Heart Attack, Gastrostomy, and Endoscopy.
McLaren Port Huron Hospital
Aiman Mahmood is a primary care provider, practicing in Internal Medicine in Port Huron, Michigan. Dr. Mahmood is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 1 other condition, according to our data. His clinical expertise encompasses Lymphangitis, Sepsis, Necrosis, Stable Angina, and Endoscopy.
Scheurer Primary Care-Caseville
Scott Reiter is a primary care provider, practicing in Family Medicine in Caseville, Michigan. Dr. Reiter is rated as an Experienced provider by MediFind in the treatment of Ornithine Transcarbamylase Deficiency. He is also highly rated in 10 other conditions, according to our data. His clinical expertise encompasses Movement Disorders, Parkinson's Disease, Urinary Tract Infection in Children, Familial Hypertension, and Hip Replacement. Dr. Reiter is currently accepting new patients.
Last Updated: 09/19/2026