Overview
Mark Hannibal is a Pediatrics specialist and a Medical Genetics provider in Ann Arbor, Michigan. Dr. Hannibal is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. His top areas of expertise are Aase Syndrome, Char Syndrome, Van Maldergem Syndrome, and C Syndrome.
His clinical research consists of co-authoring 28 peer reviewed articles. MediFind looks at clinical research from the past 15 years.
Insurance
Accepted insurance can change. Please verify directly with the provider.
Accepted insurance plans:
- EPO
- HMO
- POS
- PPO
- HMO
- INDEMNITY
- POS
- PPO
- HMO
- OTHER MEDICAID
- STATE MEDICAID
- EPO
- PPO
- HMO
- POS
- EPO
- HMO
- POS
- PPO
Locations
1500 E Medical Ctr, Suite 0331, Ann Arbor, MI 48109
1500 E Medical Ctr Dr, Ann Arbor, MI 48109
Additional Areas of Focus
Dr. Hannibal has provided the following conditions as areas of focus. Please note that we may not have enough data to validate their experience in some of these conditions.
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Regents Of The University Of Michigan
Kristen Lee is a Medical Genetics specialist and a Pediatrics provider in Ann Arbor, Michigan. Dr. Lee is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Biotinidase Deficiency, Delayed Growth, Beta-Ketothiolase Deficiency, and Triple X Syndrome.
Regents Of The University Of Michigan
Tomoyasu Higashimoto is a Medical Genetics provider in Ann Arbor, Michigan. Dr. Higashimoto is rated as an Advanced provider by MediFind in the treatment of HNRNPH2-Related Disorder. His top areas of expertise are Nevoid Basal Cell Carcinoma Syndrome, Methylmalonic Acidemia, Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, and Propionic Acidemia.
Kristin Monaghan is a Medical Genetics provider in Detroit, Michigan. Dr. Monaghan is rated as a Distinguished provider by MediFind in the treatment of HNRNPH2-Related Disorder. Her top areas of expertise are Hypotonia, 1p36 Deletion Syndrome, Microcephaly Deafness Syndrome, and Early Infantile Epileptic Encephalopathy.
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
- Distinguished
- Aase SyndromeDr. Hannibal isDistinguished. Learn about Aase Syndrome.
- Advanced
- 15q11.2 MicrodeletionDr. Hannibal isAdvanced. Learn about 15q11.2 Microdeletion.
- 2q37 Deletion SyndromeDr. Hannibal isAdvanced. Learn about 2q37 Deletion Syndrome.
- 3MC SyndromeDr. Hannibal isAdvanced. Learn about 3MC Syndrome.
- 3p Deletion SyndromeDr. Hannibal isAdvanced. Learn about 3p Deletion Syndrome.
- 47 XYY SyndromeDr. Hannibal isAdvanced. Learn about 47 XYY Syndrome.
- 5-Alpha Reductase DeficiencyDr. Hannibal isAdvanced. Learn about 5-Alpha Reductase Deficiency.
- Experienced
- AcheiropodyDr. Hannibal isExperienced. Learn about Acheiropody.
- AchondroplasiaDr. Hannibal isExperienced. Learn about Achondroplasia.
- Acro-Pectoro-Renal Field DefectDr. Hannibal isExperienced. Learn about Acro-Pectoro-Renal Field Defect.
- AcrocephalopolydactylyDr. Hannibal isExperienced. Learn about Acrocephalopolydactyly.
- AcrodysostosisDr. Hannibal isExperienced. Learn about Acrodysostosis.
- Acrofacial Dysostosis Catania TypeDr. Hannibal isExperienced. Learn about Acrofacial Dysostosis Catania Type.