Category:Pathophysiology
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Physiological processes associated with disease or injury.
Subcategories
This category has the following 10 subcategories, out of 10 total.
B
- Brain/Neurology (108 P)
C
- Cardiac Pathophysiology (76 P)
D
- Digestive Organs Pathophysiology (32 P)
E
- Endocrine Pathophysiology (31 P)
G
- Gastrointestinal Pathophysiology (48 P)
H
- Heme Pathophysiology (32 P)
O
- OB/Gyn Pathophysiology (9 P)
P
- Pediatric Pathophysiology (51 P)
- Pulmonary Pathophysiology (29 P)
R
- Renal Pathophysiology (37 P)
Pages in category "Pathophysiology"
The following 200 pages are in this category, out of 451 total.
(previous page) (next page)H
- Hepatorenal syndrome (HRS)
- Hereditary elliptocytosis
- Hereditary hemorrhagic telangiectasia (HHT)
- Hereditary pyropoikilocytosis (HPP)
- Hereditary spherocytosis
- Hernia
- Herniated Discs
- Hiatal hernia
- High-molecular-weight kininogen (HMWK or HK) Deficiency
- Hirschsprung's disease (HD or HSCR)
- Huntington's disease (HD)
- Hydrocephalus Notes
- Hyperammonemia
- Hyperhidrosis
- Hyperkalemia
- Hypernatremia
- Hyperosmolar hyperglycemic state (HHS)
- Hyperparathyroidism
- Hypertension
- Hyperthyroidism
- Hypertrophic cardiomyopathy (HCM, HOCM)
- Hyperuricemia
- Hypocalcemia
- Hypoglycemia
- Hypokalemia
- Hyponatremia
- Hypoplasminogenemia (plasminogen deficiency type 1)
- Hypospadias Notes
- Hypothyroidism
I
J
K
L
- Lambert–Eaton myasthenic syndrome (LEMS)
- Large Bowel Obstruction
- Laryngeal cleft (laryngotracheoesophageal cleft)
- Laryngomalacia
- Left Anterior Fascicular Block (LAFB)
- Left ventricular assist device (LVAD)
- Leigh syndrome
- Limb girdle syndrome
- Liver Disease Summary
- Liver Transplant Summary
- Long QT syndrome (LQTS)
- Lown–Ganong–Levine syndrome (LGL)
- Lung Transplant Notes
- Lymphangioleiomyomatosis (LAM)
M
- Macroglossia
- Malignant hyperthermia (MH)
- Mallory–Weiss syndrome
- Marfan syndrome (MFS)
- Marginal artery of the colon (marginal artery of Drummond)
- McCune–Albright syndrome
- Meckel's diverticulum
- Mediastinal tumors
- Mediastinitis
- Megacolon (toxic)
- Meige's syndrome
- MELAS syndrome
- Meningioma
- Meralgia paraesthetica
- MERRF syndrome (or myoclonic epilepsy with ragged red fibers)
- Methemoglobinemia
- Mitochondrial DNA depletion syndrome (MDS, MDDS, Alper's disease)
- Mitochondrial myopathy
- Mitral Regurgitation Summary
- Mitral Stenosis Summary
- Model for End-Stage Liver Disease (MELD)
- Molar Pregnancy
- Moyamoya disease
- Multi/minicore myopathy
- Multifocal atrial tachycardia
- Multiple Sclerosis (MS)
- Multiple system atrophy
- Muscular Dystrophy
- Myasthenia gravis (MG)
- Myocardial infarction (MI)
- Myocardial Rupture
- Myotonic Dystrophy
- Myxedema
N
O
P
- Paget's disease of bone
- Pancreatic cancer
- Pantothenate kinase-associated neurodegeneration (PKAN)
- Paramyotonia congenita (PC)
- Parkinson's disease
- Parkinsonism
- Paroxysmal nocturnal hemoglobinuria (PNH)
- Paroxysmal supraventricular tachycardia (PSVT)
- Pearson syndrome
- Pectus carinatum (Pigeon Chest)
- Pectus excavatum
- Peptic ulcer disease (PUD)
- Pericardial effusion
- Pericarditis
- Peripheral artery disease (PAD)
- Peritoneal dialysis (PD)
- Peritonitis
- Peutz–Jeghers syndrome (PJS)
- Pheochromocytoma (PHEO or PCC)
- Pierre Robin sequence
- Pituitary adenoma
- Placenta Abruption Review
- Placenta accreta spectrum
- Placenta praevia
- Placental abruption
- Pleural effusion
- Pneumothorax
- Poland syndrome
- Poliomyelitis
- Polyarteritis nodosa (PAN)
- Polycystic kidney disease (PKD or PCKD)
- Polycystic ovary syndrome (PCOS)
- Polycythemia (polycythaemia, polyglobulia)
- Polycythemia vera
- Polymyositis (PM)
- Polyps
- Portal hypertension
- Portopulmonary hypertension
- Posterior urethral valve
- Postoperative cognitive dysfunction (POCD)
- Postpartum hemorrhage (PPH)
- Pre-eclampsia
- Prekallikrein (PK, Fletcher factor) Deficiency
- Premature atrial contractions (PACs)
- Premature ventricular contraction (PVC)
- Primary central nervous system lymphoma (PCNSL)
- Primary ciliary dyskinesia (Kartagener's syndrome)
- Primitive neuroectodermal tumor
- Progressive familial intrahepatic cholestasis (PFIC)
- Protein C deficiency
- Protein S deficiency
- Proteinuria
- Prune belly syndrome
- Pseudomembranous Colitis
- Pulmonary alveolar proteinosis (PAP)
- Pulmonary edema
- Pulmonary embolism (PE)
- Pulmonary hypertension
- Pyloric stenosis
R
S
- Sarcoidosis
- Schwartz–Jampel syndrome (SJS)
- Scoliosis / Kyphosis
- Seizure Physiology and Types
- Serotonin syndrome (SS)
- Serum creatinine
- Sheehan's syndrome (postpartum pituitary gland necrosis)
- Short bowel syndrome (SBS, short gut)
- Shunt - Acyanotic (Left to Right)
- Shunt - Cyanotic (Right to Left)
- Sickle cell disease (SCD)
- Sinus arrhythmia
- Situs inversus
- Slipped capital femoral epiphysis (SCFE or skiffy)
- Small Bowel Obstruction
- Spasmodic dysphonia
- Spina bifida
- Spinal stenosis