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 1,048 Multiple-choice 1st, 2nd, and 3rd order questions with four detailed teaching points linked to 382 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 (1,048)
Our question bank for the Genetics Exam covers four Cognitive Difficulty Levels:
- Allergy and Immunology - 36 questions
- Cardiovascular - 60 questions
- Connective Tissue - 22 questions
- Ears Nose and Throat - 38 questions
- Endocrine and Metabolic - 257 questions
- Eyes - 70 questions
- Gastrointestinal - 105 questions
- Genetics - 966 questions
- Genitourinary - 42 questions
- Growth and Development - 262 questions
- Gynecologic - 32 questions
- Hematologic - 119 questions
- Infectious - 35 questions
- Integument - 80 questions
- Musculoskeletal - 191 questions
- Nervous - 256 questions
- Nutrition - 12 questions
- Obstetric - 40 questions
- Oncologic - 132 questions
- Psychiatric Mental Health - 19 questions
- Pulmonary - 42 questions
- Renal - 54 questions
- Surgery - 10 questions
- Toxicology - 6 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) - 428 questions
- Process (Analysis, Assess, Eval, Implement, Plan) - 452 questions
- Caring (Hope and Support) - 3 questions
- Communication/Documentation (Oral, Written, EMR) - 2 questions
- Teaching/Learning (Promotes Behavior Change) - 3 questions
- Causes - 611 questions
- Classification - 113 questions
- Differential - 596 questions
- Epidemiology - 60 questions
- Evaluation Diagnostic Tests - 347 questions
- Evaluation Lab - 384 questions
- Evaluation Monitoring - 32 questions
- Evaluation Procedures - 137 questions
- Evaluation Radiologic - 143 questions
- Health Maint Prevention Public Health - 10 questions
- History Physical - 1046 questions
- Pathophysiology - 774 questions
- Patient Education - 35 questions
- Prognosis Complications - 498 questions
- Toxicology - 4 questions
- Treatment Medical - 85 questions
- Treatment Occupation/Physical Therapy - 2 questions
- Treatment Surgical - 23 questions
- Clinical Education - 11 questions
- Therapeutics (Drug treatment) - 17 questions
- Drug Information - 10 questions
- Pharmaceutics (Safely dosing medications) - 5 questions
- Pharmacokinetics (Drug movement in body) - 1 questions
Genetics Exam Articles (382)
Individuals with an intellectual disability have neurodevelopmental deficits characterized by limitations in
Cerebral amyloid angiopathy (CAA) is a type of cerebrovascular disorder characterized by the accumulation of amyloid beta-peptide within the leptom ...
Galactosemia is an inborn error of metabolism due to impaired degradation of galactose. The disease was first described in 1917, and defe ...
This article will give a brief overview of gastrulation, a critical process during week 3 of human development. Gastrulation is defined as an early ...
As the name implies, neurocutaneous syndromes are disorders involving the nervous system and the skin. It is essential for clinicians, especially p ...
Thalassemia and sickle cell disease are some of the most common single-gene inherited hemoglobin disorders worldwide. Unlike sickle cell disease, w ...
Spinal muscular atrophy (SMA) denotes a collection of inherited clinical syndromes causing degeneration of anterior horn cells in the spinal cord w ...
Historically, pregnancy was a very tenuous part of a woman's life because of the high mortality rate associated with gestation. In the early 1900s, ...
Perhaps biology faces no greater feat than the generation of a complex, multicellular organism from a single cell origin. The eye quintessentially ...
The entire nervous system forms via the process called neurulation in which neural tube and neural crest form initially. In the third week of embry ...
Zinc is an essential nutrient for humans and is extensively involved in protein, lipid, nucleic acid metabolism, and gene transcription. Its role w ...
Hearing loss is a common complaint for which referrals are frequently made to secondary care for an otolaryngologist's attention. There are two typ ...
Glanzmann thrombasthenia (GT), first described in 1918, is a congenital bleeding disorder caused by a defect and/or deficiency of a platelet integr ...
Caroli disease is also known as congenital communicating cavernous ectasia of the biliary tree, is a rare inherited disorder involving segment ...
Sickle cell disease (SCD) is a multisystem disorder and the most common genetic disease in the United States, affecting 1 in 500 African Americans. ...
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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