MRCP Part 1 Syllabus

MRCP(UK) Part 1 samples the whole of general internal medicine plus a substantial block of clinical sciences, across 200 best-of-five questions in two three-hour papers. This page breaks the syllabus down specialty by specialty, sets out what each area actually examines, and links each topic to the Examrix notes and questions that cover it.

The authoritative blueprint is published by the Federation of the Royal Colleges of Physicians and is revised periodically — always confirm current specialty allocations on the official Part 1 pages. The breakdown below reflects the areas the blueprint samples; it does not invent question counts or percentages.

How the MRCP Part 1 syllabus is tested

Every question is a single best answer with five options and no negative marking. The syllabus is not tested as isolated facts: a stem gives a short clinical vignette with a focused set of findings, and you are asked for the most likely diagnosis, the next investigation, the best management step or the underlying mechanism.

Clinical sciences and pharmacology are woven through the clinical specialties rather than sitting in a separate section of the paper — a cardiology question can turn on a receptor mechanism, and a gastroenterology question on drug metabolism. Data interpretation is constant: gases, renal and liver profiles, thyroid function, autoantibody panels and described ECGs.

The paper also expects familiarity with current UK national guidance, so learn thresholds and first-line choices as specific numbers and drugs rather than general impressions.

MRCP Part 1 syllabus: topic breakdown

Topic names link to the free Examrix revision note covering that area where one is available.

Cardiology

Vignettes centre on ECG interpretation, murmurs and the acute coronary and arrhythmia pathways, usually with one discriminating investigation result.

  • ECG patterns: ischaemia, blocks, pre-excitation, long QT
  • Acute coronary syndromes and heart failure management
  • Valve lesions, murmurs and endocarditis
  • Arrhythmias, inherited channelopathies and sudden cardiac death
  • Adult congenital and structural lesions

Free notes: ECG, Exercise Testing and Cardiac Biomarkers · Inherited Arrhythmia and Sudden Cardiac Death Syndromes · Congenital Heart Disease: Shunts and Structural Lesions

Respiratory medicine

Expect spirometry and blood gas interpretation attached to a short history, plus guideline-driven escalation questions.

  • Obstructive versus restrictive spirometry and transfer factor
  • Asthma and COPD escalation to current UK guidance
  • Interstitial lung disease patterns and occupational exposures
  • Pleural fluid analysis and Light's criteria
  • Pulmonary embolism, pulmonary hypertension and sleep-disordered breathing

Free notes: Interstitial Lung Disease

Gastroenterology and hepatology

Liver screens, inflammatory bowel disease and upper GI bleeding scoring recur; the discriminator is usually a single serology or biochemistry result.

  • Liver screen interpretation and chronic liver disease aetiology
  • Decompensated cirrhosis: ascites, encephalopathy, variceal bleeding, SBP
  • Inflammatory bowel disease: diagnosis, flares and biologics
  • Malabsorption, coeliac disease and pancreatic insufficiency
  • Upper GI bleeding risk scores and endoscopic management

Free notes: Chronic Liver Disease · Decompensated Cirrhosis

Endocrinology and diabetes

Dynamic function tests are the backbone of this area: you are shown a set of results and asked what they mean or what to do next.

  • Thyroid disease including thyrotoxicosis, myxoedema and amiodarone effects
  • Adrenal disease: Cushing's, Addison's, phaeochromocytoma, incidentaloma
  • Diabetic emergencies — DKA and hyperosmolar hyperglycaemic state
  • Calcium, parathyroid and bone metabolism
  • Pituitary disease, MEN syndromes and hyponatraemia workup

Free notes: Thyrotoxicosis and Hypothyroidism · Adrenal Disease · Diabetic Emergencies · Calcium Disorders

Nephrology

Acid–base and electrolyte questions are highly learnable and appear across the whole paper, not only in renal-labelled items.

  • Acute kidney injury: causes, staging and reversible factors
  • Chronic kidney disease complications and replacement therapy indications
  • Acid–base algorithm, anion gap and compensation
  • Sodium, potassium, calcium and magnesium disorders
  • Glomerulonephritis patterns and their serological associations

Free notes: Acute Kidney Injury · CKD Complications and Treatment · Acid-Base Disorders

Neurology

Localisation is the core skill: the stem gives an examination pattern, and the answer follows from where the lesion must be.

  • Stroke syndromes, TIA risk and secondary prevention
  • Cranial nerve and spinal cord localisation
  • Movement disorders and parkinsonian syndromes
  • Neuromuscular disease, neuropathies and myasthenia
  • Epilepsy management, CSF patterns and CNS infection

Free notes: Stroke and TIA · Movement Disorders · Clinical Neuroanatomy

Rheumatology

Autoantibody profiles do most of the discriminating work; learn the specific associations rather than broad patterns.

  • Connective tissue disease: SLE, systemic sclerosis, myositis, Sjögren's
  • Vasculitides and their ANCA associations
  • Crystal arthropathies and septic arthritis
  • Rheumatoid arthritis, DMARDs and monitoring requirements
  • Spondyloarthropathies and extra-articular features

Free notes: Connective-Tissue Disease Overview

Infectious diseases

Most items map an organism to a syndrome, an exposure or a host defect, then ask for the antimicrobial or the confirmatory test.

  • Sepsis recognition and initial management
  • Skin, soft-tissue, bone and joint infection
  • HIV: opportunistic infections, CD4 thresholds and antiretroviral effects
  • Tropical and travel-related infection
  • Tuberculosis, endocarditis and antimicrobial resistance mechanisms

Free notes: Sepsis · Skin and Soft-Tissue Infection

Haematology

Blood film and marrow descriptions carry the diagnosis; the rest of the stem usually confirms rather than reveals.

  • Anaemias: microcytic, macrocytic and haemolytic patterns
  • Transfusion medicine and transfusion reactions
  • Coagulation disorders, thrombophilia and anticoagulation
  • Myeloproliferative and myelodysplastic disorders
  • Myeloma, lymphoma and leukaemia recognition

Free notes: Microcytic Anaemia · Transfusion Medicine

Oncology and palliative care

Emergencies and symptom control dominate — the exam tests the physician's role rather than oncological staging detail.

  • Oncological emergencies: cord compression, SVC obstruction, neutropenic sepsis, hypercalcaemia
  • Tumour lysis syndrome and treatment toxicities
  • Paraneoplastic syndromes
  • Opioid conversion and symptom control at the end of life
  • Cancer of unknown primary and screening principles

Free notes: Oncological Emergencies · Palliative Symptom Control

Dermatology

A small block with narrow, well-defined content — usually the skin sign of a systemic disease or a drug eruption.

  • Skin cancer recognition and management
  • Cutaneous signs of systemic and endocrine disease
  • Drug eruptions including SJS/TEN and DRESS
  • Blistering disorders and psoriasis therapy

Free notes: Skin Cancer

Medical ophthalmology

Confined to the eye problems a physician meets: the red eye, sudden visual loss and fundal findings in systemic disease.

  • The red and painful eye
  • Sudden visual loss and visual field defects
  • Diabetic and hypertensive retinopathy
  • Ocular features of inflammatory and thyroid disease

Free notes: Red Eye and Painful Eye

Psychiatry and geriatric medicine

Tested from the medical ward perspective: capacity, delirium, falls and psychotropic side effects.

  • Depression, suicide risk assessment and antidepressant choice
  • Delirium versus dementia and the confused inpatient
  • Capacity, consent and the relevant legal frameworks
  • Falls, frailty and polypharmacy in older patients
  • Psychotropic adverse effects including serotonin syndrome and NMS

Free notes: Depressive Disorders and Suicide Risk · Falls and Mobility

Clinical pharmacology, therapeutics and toxicology

A consistently large and consistently under-prepared area. Numbers matter here: thresholds, half-lives and antidote doses.

  • Pharmacokinetics, pharmacodynamics and therapeutic drug monitoring
  • Cytochrome P450 inducers, inhibitors and clinically important interactions
  • Prescribing in pregnancy, renal and hepatic impairment and in older people
  • Adverse drug reactions and drug-induced organ injury
  • Poisoning and antidotes: paracetamol, salicylate, lithium, digoxin, carbon monoxide, TCAs

Free notes: Prescribing in Special Populations

Basic sciences and statistics

The clinical sciences block is discrete, finite and stable, which makes it the most reliable source of marks per hour in the whole paper.

  • Cell and membrane physiology: channels, transport, action potentials
  • Fluid, electrolyte and acid–base physiology
  • Immunology: hypersensitivity, complement, cytokines, immunodeficiency
  • Genetics: inheritance patterns, imprinting, trinucleotide repeats
  • Metabolism and biochemistry, and relevant clinical anatomy
  • Statistics and epidemiology: sensitivity, specificity, predictive values, NNT, study design and bias

Free notes: Cell Membrane Physiology · Fluid, Electrolyte and Acid-Base Physiology · Immune Response · Genetic Principles · Metabolism · Diagnostic Test Performance

How to prioritise high-yield topics

No specialty is large enough to carry the paper, so breadth beats depth. The practical question is not which area is biggest, but which converts study hours into marks most reliably.

  • Bank the finite topics early. Statistics, genetics, immunology, acid–base and toxicology have small, stable content and are examined every diet.
  • Do not skip the small specialties. Dermatology, ophthalmology, psychiatry and geriatric medicine contribute modest numbers of questions from very narrow content — a focused session each usually converts most of those marks.
  • Weight your second pass by your own data, not by blueprint size. After one pass across everything, your per-topic accuracy tells you where the marks are being lost. Spend the second pass on the areas furthest below your average.
  • Revise around discriminators. For each condition, learn the one or two features that separate it from its nearest mimic and the first-line management, rather than exhaustive lists.

How to combine syllabus coverage with question-bank practice

Reading alone does not reveal whether you can apply a topic under exam conditions. The most efficient pattern is to read a syllabus area, then immediately do 20–30 questions on it in untimed tutor mode, reading every explanation including for the options you rejected.

Once the first pass is complete, move to mixed random blocks so you practise recognising which area a question belongs to — a skill the specialty-by-specialty structure of this page deliberately removes. In the final four to six weeks, add full-length timed papers to build pacing and stamina.

Track coverage as well as accuracy. Per-topic analytics show both which syllabus areas you have barely touched and which ones you are consistently getting wrong; those are different problems with different fixes.

Cover the syllabus with the Examrix MRCP Part 1 question bank

Every Examrix question is mapped to a syllabus area, with a full explanation, timed exam-style practice and analytics that show your coverage and accuracy across every specialty above.

More MRCP Part 1 resources