Our review is designed to help you maximize your score on the Genetics Exam. StatPearls questions and articles are linked directly to NBME® and NBOME® content outlines. Each review course is designed to empower you to assess your knowledge and understanding of medical principles and concepts found on the Genetics Exam.
We have 1,035 Multiple-choice 1st, 2nd, and 3rd order questions with four detailed teaching points linked to 381 PubMed indexed review articles related to the Genetics Examination. You can customize practice questions to anatomical and clinical Genetics Medical Student subject areas. In addition, you will have access to a 250 question pre- and post-test Genetics Exam to help you target learning and identify areas that need further study. Analytics and reports allow you to compare your scores to other students.
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The StatPearls genetics practice exam questions, genetics shelf assessment questions, genetics practice test questions, and genetics shelf exam questions will help you achieve a top score on the Genetics Examination. 416 authors and 12 editors have contributed to the development of the Genetics Exam content, which is continuously refined and updated to improve your learning experience.
Genetics Exam Overview
How many hours is the Genetics Exam?
The Genetics Exam is 2.5 hours.
How many questions is the Genetics Exam?
The Genetics Exam is 125 questions.
What topics are covered on the Genetics Exam?
Topics include: The Genetics exam is designed to assess performance at the end of a course, clerkship, or other unit of instruction.
Genetics Exam MCQs (1,035)
Our question bank for the Genetics Exam covers four Cognitive Difficulty Levels:
- Allergy and Immunology - 35 questions
- Cardiovascular - 59 questions
- Connective Tissue - 22 questions
- Ears Nose and Throat - 38 questions
- Endocrine and Metabolic - 254 questions
- Eyes - 69 questions
- Gastrointestinal - 103 questions
- Genetics - 949 questions
- Genitourinary - 44 questions
- Growth and Development - 257 questions
- Gynecologic - 33 questions
- Hematologic - 114 questions
- Infectious - 35 questions
- Integument - 78 questions
- Musculoskeletal - 188 questions
- Nervous - 250 questions
- Nutrition - 12 questions
- Obstetric - 39 questions
- Oncologic - 126 questions
- Psychiatric Mental Health - 18 questions
- Pulmonary - 43 questions
- Renal - 54 questions
- Surgery - 10 questions
- Toxicology - 5 questions
- Trauma - 3 questions
- Manage Care and Comply Regulations - 3 questions
- Health Promotion & Maintenance (Prevent Problems) - 16 questions
- Pharm/Parenteral Therapy (Drugs/Vital Signs) - 21 questions
- Reduction Risk (Post Procedure) - 4 questions
- Physiological Adaptation (Care Ill Patients) - 417 questions
- Process (Analysis, Assess, Eval, Implement, Plan) - 440 questions
- Caring (Hope and Support) - 3 questions
- Communication/Documentation (Oral, Written, EMR) - 2 questions
- Teaching/Learning (Promotes Behavior Change) - 3 questions
- Causes - 605 questions
- Classification - 116 questions
- Differential - 586 questions
- Epidemiology - 60 questions
- Evaluation Diagnostic Tests - 343 questions
- Evaluation Lab - 377 questions
- Evaluation Monitoring - 33 questions
- Evaluation Procedures - 132 questions
- Evaluation Radiologic - 141 questions
- Health Maint Prevention Public Health - 10 questions
- History Physical - 1032 questions
- Pathophysiology - 764 questions
- Patient Education - 35 questions
- Prognosis Complications - 491 questions
- Toxicology - 3 questions
- Treatment Medical - 84 questions
- Treatment Occupation/Physical Therapy - 2 questions
- Treatment Surgical - 23 questions
- Clinical Education - 11 questions
- Therapeutics (Drug treatment) - 18 questions
- Drug Information - 10 questions
- Pharmaceutics (Safely dosing medications) - 5 questions
- Pharmacokinetics (Drug movement in body) - 1 questions
Genetics Exam Articles (381)
Ehlers Danlos syndrome (EDS) is a group of hereditary connective tissue disorders which manifests clinically with skin hyperelasticity, h ...
Hereditary non-polyposis colorectal cancer (HNPCC), also known as Lynch syndrome, is an autosomal dominant trait and the most common cause of inher ...
Glanzmann thrombasthenia (GT), first described in 1918, is a congenital bleeding disorder caused by a defect and/or deficiency of a platelet integr ...
Myotonic dystrophy (DM) is considered a subgroup of myopathy and the most common type of muscular dystrophy that begins in adulthood. There are two ...
Lipoprotein disorders are clinically important due to the of the role of lipoproteins in atherogenesis and the associated risk of atherosclerotic c ...
Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder characterized by the development of multiple tumors involving the central ner ...
Multiple Endocrine Neoplasia Type 1 (MEN1) is a rare endocrine tumor syndrome with high penetrance. This syndrome is also known as Wermer Syndrome. ...
Persistent truncus arteriosus (TA) is a rare, congenital, cyanotic heart defect characterized by a ventricular septal defect (VSD), a single trunca ...
Pancreatic cancer refers to the carcinoma arising from the pancreatic duct cells, pancreatic ductal carcinoma. It is the fourth leading cause ...
In 1969, a remarkable cancer predisposition syndrome was reported by Li and Fraumeni. Li-Fra ...
The foot is a complex anatomic structure composed of numerous bones, joints, ligaments, muscles, and tendons responsible for the complex coordinate ...
The amniotic fluid index is a standardized way to assess the sufficiency of amniotic fluid quantity in pregnancy. The amniotic fluid index is used ...
Friedreich ataxia (FA) is the most common hereditary ataxia accounting for approximately 50% of all ataxia cases.
Trisomy 13 was first described as the cause of a distinct clinical syndrome in 1960 by Dr. Patau et al.
Hodgkin lymphoma characteristically presents with Hodgkin and Reed-Sternberg cells. When the cells are mononucleated, they are called Hodgkin cells ...
Melissa Henderson PhD Assistant Professor Lincoln Memorial Uni, DeBusk College Harrogate TN
Divya Khattar MD Cincinnati Children’s Hospital Medical Center, Cincinnati, OH Cincinnati OH
Brittany Simpson MD Fellow Cincinnati Children's Hospital Cincinnati OH
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