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- Disease Information
- Disease Comparison
-
Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
- Electromagnetic-Physics
- Eponymic
- Functional-Physiologic
- Hereditofamilial
- Iatrogenic
- Idiopathic
- Infected Organ-Abcess
- Infectious agent
- Inflammatory-Granulomatous
- Metabolic-Storage
- Neoplastic
- Poison Agent
- Poisoned Organ
- Radiation-Xray-trauma
- Mental
- Structural-Anatomic-Foreign body
- Surgical Procedure-Complication
- Trauma
- Use-age-Atrophic
- Endocrine-Vegetative
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Comparison Results (show differences mode) for Paroxysmal Nocturnal Hemoglobinuria and Renal Failure Acute
Found: 196 | Differences: 187
Paroxysmal Nocturnal Hemoglobinuria
Found: 214 | Differences: 205Paroxysmal Nocturnal Hemoglobinuria and Renal Failure Acute sharing 8 common findings. (show all, show common, show differences)
- Clinical Manifestations
- Signs & Symptoms
- Edema Children
- Facial edema/swelling
- Diastolic hypertension
- Fluid retention/Mild edema
- High blood pressure/sign
- Tachycardia/Fast heart rate
- Beau's lines/Mees lines fingernails
- Bruising/Ecchymosis
- Nail Striations
- Petechiae/Petechial rash
- Pruritis Itching
- Excessive/easy bruising tendency
- Anorexia Decreased appetite
- Hiccough/Hiccups
- Nausea
- Vomiting
- Breath odor of Ammonia
- Characteristic breath odor
- Dry mouth/Mucous membranes
- Metallic taste
- Liver flap tremor/Asterixis
- Chvostek's sign
- Cramping in Extremities
- Muscle fasciculations
- Muscle twitches
- Muscle weakness
- Twitchy/muscle spasms
- Weak/Weak as a kitten (symptom)
- Altered Mental State Diabetic
- Altered mental status Mental status change
- Confusion/agitation on exam
- Confusion/Disoriented
- Fatigability
- Infant Seizures
- Lethargy/torpor
- Myoclonus/Myoclonic jerks on exam
- Obtunded/poorly responsive status/signs
- Seizures
- Seizures/Children/recurrent
- Stupor/poor reponse to stimulus
- Sudden unconsciousness
- Weakness/Diffuse motor loss
- Hyperpnea
- Rapid Breathing
- Tachypnea/Increased respiratory rate
- Chronic Back Pain
- Epistaxis, severe/persistent
- Anuria
- Breath odor of Stale fish
- Oliguria/Decreased urine output
- Oliguria/sudden
- Uremic fetor
- Acutely ill patient/signs
- Chronic Fatigue
- Enervated/extreme acute fatigue
- Fatigue Tiredness Exhaustion
- Neonatal edema/anasarca
- Weakness
- Weakness non-neuromuscular/systemic
- Weight gain
- Weight Loss
- Eyelid Fasciculations
- Retinopathy signs on exam
- Clinical Presentation & Variations
- Presentation/Hypertension Abrupt Onset
- Presentation/Diabetic Decreased need for Insulin
- Disease Progression
- Course/Acute
- Course/Acute only
- Course/Potentially lethal/untreated
- Lethal Potential
- Demographics & Risk Factors
- Established Disease Population
- Patient/Bacterial endocarditis
- Patient/Preeclampsia/toxemia
- Patient/Shock status
- Patient/Severe/extensive Burns
- Patient/Glomerulonephritis, acute
- Laboratory Tests
- Abnormal Lab Findings (Non Measured)
- Hyperprolactinemia
- Osmotic gap (low Na/high osmolality) (Lab)
- Renal function abnormalities (Lab)
- Abnormal Lab Findings - Decreased
- Aspartamine aminotransferase (SGOT, AST) (Lab)
- Bicarbonate, serum (Lab)
- Calcium, serum (Lab)
- Carbon Dioxide Total Content/CO2
- Creatine clearance (Lab)
- Lymphocytes (Lab)
- PCO2, arterial blood (Lab)
- pH, arterial blood (Lab)
- Sodium, serum (Lab)
- URINE Osmololality
- URINE Potassium
- Abnormal Lab Findings - Increased
- Acute lymphopenia/transient
- Brain Natiuretic Peptide/BNP level (Lab)
- BUN/Blood urea nitrogen (Lab)
- Creatinine, serum (Lab)
- Digoxin serum level (Lab)
- Fibrin Degredation Product (FDP) (Lab)
- Fibrin Split Products/FSP/Dimers/Monomers (Lab)
- Fibrinopeptide A
- FibrinPeptide A
- Free fatty acids/FFA/Non-esterified (Lab)
- Gastrin, serum (Lab)
- Glucagon (Lab)
- Growth hormone/STH, plasma (Lab)
- Lactic acid/Lactate (Lab)
- Lipase (Lab)
- Magnesium (Lab)
- NT-proBNP indicator levels (N-terminal)
- Phosphate Serum (Lab)
- Potassium, serum (Lab)
- Prolactin (Lab)
- Sodium, serum (Lab)
- Sulfate, serum (Lab)
- Triglyceride lipase (Lab)
- Uric acid, serum (Lab)
- URINE Glucuronidase, beta
- URINE Growth hormone
- URINE Hexosaminidase
- URINE Protein (Albumin)
- Diagnostic Test Results
- Isotope Scan
- Isotope/DMAS Kidney Scan Abnormal
- EKG (ECG)
- EKG/Prolonged QT interval (ECG)
- EKG/Prolonged QT/Peaked T Waves (ECG)
- X-RAY
- Xray/Chest abnormal
- Xray/Congestive heart failure signs/Chest
- Xray/Chest/Lung fields/Abnormal
- Xray/Lung consolidation/Chest
- X-RAY With contrast
- IVP/Decreased dye visualization/bilateral
- IVP/Dense nephrogram, bilateral
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Hyperkalemic periodic paralysis
- Myxedema coma
- Associated Disease & Complications - Causes
- Acidosis
- Acidosis, metabolic
- Acute anuria/renal failure
- Azotemia in Children
- Azotemia in Elderly
- Azotemia/Acute
- Congestive heart failure
- Convulsions (grand mal)
- Death Outcome
- Digitalis toxicity/poisoning
- Gastrointestinal bleeding
- Hallucinations
- Hyperkalemia
- Hypermagnesemia
- Hypernatremia
- Hyperphosphatemia
- Hypertension
- Hyperuricemia
- Hypervolemia
- Hypocalcemia
- Hypocapnea/hypocarbia
- Hyponatremia
- Intravenous pyelogram CONTRA-INDICATED/DANGER
- Lactic acidosis
- Lymphocytopenia
- Metabolic Acidosis with High Anion Gap
- Metabolic encephalopathy
- Pneumonia, pneumococcal
- Pneumonia, staphylococcus
- Potassium administration/effect/toxicity
- Proteinuria
- Retinopathy
- Sideroblastic Anemia Sideroachrestic
- Xerostomia
- Hypergastrinemia
- Disease Synergy
- Synergy/Digitalis/digoxin toxicity
- Synergy/On medications/medication
- Synergy/Salt load/high sodium diet
- Disease Mechanism & Classification
- Class
- CLASS/Renal/kidney involvement/disorder (ex)
- CLASS/Urologic (category)
- Pathophysiology
- Pathophysiology/Blood volume/increase/high
- Pathophysiology/Alveolar consolidation
- Pathophysiology/Decreased glomerular filtration
- Pathophysiology/Salt/water retention, renal
- Process
- PROCESS/Complicating disorder (ex)
- PROCESS/Non-hereditary metabolic disorder (ex)
- Synonyms
- Synonym
- Synonym/ARF
- Synonym/Azotemia
- Treatment
- Drug Therapy - Contraindication
- RX/Diuretic
- RX/Magnesium oxide
- RX/Potassium-sparing diuretic
- Other Treatments
- TX/Dialysis.
- TX/Fluid restriction
- TX/Medical emergency
- Clinical Manifestations
- Signs & Symptoms
- Paroxysmal Shivering
- Rigors/Shaking chills
- Teeth Chattering
- Uncontrollable Shaking
- Abdominal pain Radiates to Back
- Recurrent Abdominal Pain
- Stroke Syndrome Child
- Mid-back pain
- AM dark urine/on awakening
- Coca-Cola dark (coffee colored) urine
- Costovertebral Angle Pain/Tenderness
- Dark urine
- Flank Pain
- URINE Color Red
- Massive splenomegaly
- Splenomegaly
- Chills
- Nocturnal awakenings Events Phenomenon
- Otherwise well Isolated problem
- Pallor
- Clinical Presentation & Variations
- Presentation/Deep Vein Thrombosis Young Recurrent
- Presentation/Anemia Refractory
- Presentation/Refractory iron deficiency anemia
- Disease Progression
- Course/Attacks Episodic Spells
- Course/Chronic disease crisis/flare/attacks
- Course/Chronic disorder
- Course/Chronic only
- Course/Episodes last 1 to 3 weeks/remit recur months later
- Course/Paroxysmal
- Course/Periodic Episodic
- Course/Prognosis bad/usually
- Pancytopenia with Hypercellular Marrow
- Pancytopenia with Normal Marrow
- Demographics & Risk Factors
- Population Group
- Child
- Population/Pediatrics population
- Family History
- Family history/Anemia
- Sex & Age Groups
- Population/Adult ('twenties')
- Population/Adult Aged Only
- Population/Adult/all
- Population/Child
- Population/Children/all
- Population/Male
- Laboratory Tests
- Microbiology & Serology Findings
- Reticulocytosis
- Abnormal Lab Findings (Non Measured)
- Cytogenetics Abnormal
- Acid hemolysis test (Ham) positive (Lab)
- Chromosomal abnormality (Lab)
- Coombs negative hemolytic anemia (Lab)
- Flow cytometry tests/abnormal (Lab)
- Flow Cytometry/CD55 and CD59 defects (Lab)
- Indirect bilirubin inc/normal direct bil. (Lab)
- Leukopenia
- Microcytes/small RBCs on Blood smear
- Microcytosis/microcytic anemia (Lab)
- Normocytic anemia
- Normocytic Anemia/High Retic count
- Normocytic/Normochromic Anemia (Lab)
- PI-linked Antigen (Cd14/CD59) positive
- Sucrose-water hemolysis test/abnormal (Lab)
- URINE Color Brown
- URINE Dipstick /Blood abnormal
- Abnormal Lab Findings - Decreased
- Ferritin, serum (Lab)
- Hematocrit (Lab)
- Hemoglobin (Lab)
- Iron, serum (Lab)
- Leukocyte Alkaline phosphatase (Lab)
- MCV/Mean Corpuscular Volume (Lab)
- Platelet survival (Lab)
- RBC/Red Blood Count (Lab)
- Abnormal Lab Findings - Increased
- Bilirubin, serum (Lab)
- C3, serum (Lab)
- Fetal hemoglobin (Lab)
- Free hemoglobin, plasma (Lab)
- Indirect bilirubin (Lab)
- Lactic Dehydrogenase (LDH LH) (Lab)
- Leukocyte Alkaline phosphatase (Lab)
- Methemalbumin (Lab)
- Osmotic fragility, RBC (Lab)
- Platelet Antibody Detection
- Polychrome RBCs (Lab)
- RBC Actylcholinesterase level (Lab)
- Reticulocytes (Lab)
- Spherocytes (Lab)
- TIBC/Total Iron Binding capacity (Lab)
- URINE Hemoglobin
- URINE Hemosiderin
- URINE Red blood cells
- URINE Urobilinogen
- STOOL Urobilinogen
- Diagnostic Test Results
- Pathology
- Bone Marrow/Erythroid hyperplasia
- Bone Marrow/Hypercellular
- Bone Marrow/Normoblasts hyperplasia
- BX/Renal hemosiderosis
- PATH/Erythrophagocytosis/Spleen
- Associated Diseases & Rule outs
- Associated Disease & Complications - Rule Outs
- Hemolytic anemia/autoimmune
- Myelodysplasia
- Associated Disease & Complications - Causes
- Acute Myelogenous/Myeloblastic Leukemia AML
- Acute Tubular Necrosis
- Anemia
- Anemia, aplastic
- Anemia, severe
- Arterial Occlusion
- Bilirubinemia
- Bone Marrow Fibrosis
- Brisk Hemolysis/Active
- Cavernous sinus thrombosis
- Cerebral thrombosis
- Cerebral vein thrombosis/phlebitis
- Cholelithiasis
- Disseminated intravascular coagulation
- Folic acid deficiency anemia
- Hemoglobinuria
- Hemolysis anemia/acute/active
- Hepatic vein thrombosis (Budd-Chiari)
- Hypercoagulability/Thrombophilia
- Iron deficiency anemia
- Leukemia
- Mesenteric vein thrombosis
- Myelodysplasia
- Myelofibrosis
- Myelofibrosis secondary
- Pancytopenia
- Paroxysmal nocturnal hemoglobinuria
- Phlegmasia cerulea dolens
- Portal vein thrombosis
- Priapism/persistent erection
- Pulmonary embolism
- Pulmonary infarction
- Purpura fulminans
- Raynaud's syndrome
- Renal Failure Chronic
- Stroke/Child
- Thrombocytopenia
- Thrombocytopenia in Children
- Thrombocytopenia in Elderly
- Thromboembolic disease
- Thrombophlebitis Arm/Deep Vein
- Thrombophlebitis, deep vein
- Thrombosis, arterial
- Thrombosis, renal vein
- Phlebitis, recurrent
- Hypercoaguability
- Disease Synergy
- Synergy/Immunizations/vaccinations
- Synergy/Infection
- Synergy/Iron ingestion/administration
- Synergy/Menses trigger
- Disease Mechanism & Classification
- Class
- CLASS/Primary organ/system disorder (ex)
- CLASS/Erythrocyte disorder (ex)
- CLASS/Hematologic (category)
- CLASS/Stem cell disease (ex)
- Pathophysiology
- Pathophysiology/Chromosome gene/segment deletion (ex)
- Pathophysiology/Gene locus Chromosome X.
- Pathophysiology/Gene Locus Identified/OMIM database
- Pathophysiology/Gene locus PIG-A gene /X-chromosome
- Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
- Pathophysiology/Arterial Occlusion
- Pathophysiology/Thrombosis veins lower ext/iliac/femoral
- Pathohysiology/PIGA defect/GPI Membrane Anchor fails
- Pathophysiology/Chronic Iron loss
- Pathophysiology/Complement sensitivity
- Pathophysiology/Erythrocyte membrane disorder
- Pathophysiology/Hemolysis
- Pathophysiology/Hemolytic process/effect
- Pathophysiology/Intrinsic CO production increased
- Pathophysiology/Myelodysplasia process
- Pathophysiology/Non-immune hemolytic anemia
- Pathophysiology/Plasma c3b inactivatior/failure
- Pathophysiology/RBC membrane defect/complement risk
- Pathophysiology/RBC membrane glycosyl-phosphatidyl-inositol path
- Pathophysiology/RBC membrane/Missing key proteins
- Pathophysiology/Stem cell defect
- Pathophysiology/Unusual sensitive RBC to C3 in plasma
- Pathophysiology/Complement activation
- Pathophysiology/Granulocyte lyses/manifestation
- Process
- PROCESS/Allergy/collagen/autoimmune (category)
- PROCESS/Episodic disorder (ex)
- PROCESS/Hereditofamilial (category)
- PROCESS/Idiopathic/unclassified/unknown (category)
- PROCESS/INCIDENCE/Acquired disorder
- PROCESS/INCIDENCE/Rare disease (ex)
- PROCESS/Pre-Leukemic condition (ex)
- PROCESS/Coagulation derangement/disorder (ex)
- PROCESS/Somatic mutation/not hereditary
- Synonyms
- Synonym
- Synonym/Marchiafava-Micheli syndrome
- Synonym/PNH
- Treatment
- Drug Therapy - Contraindication
- RX/Oral contraceptive
- Drug Therapy - Indication
- RX/Blood transfusion/packed cells
- RX/Eculizamab (Soliris)
- RX/Folic/Folinic acid (Leukovorin)
- RX/Iron/Ferrous Sulfate (Feosol)
- RX/Prednisone (Deltasone)
- SX/Bone marrow transplant
- SX/Stem cell transplant/allogenic
- SX/Stem-cell transplant
- Other Treatments
- TX/Platelet transfusion