Disease Comparison Results (show all mode) for Heparin cofactor 2 deficiency and Von Willebrand's disease

Ads

Von Willebrand's disease

Found: 129 | Differences: 117

Heparin cofactor 2 deficiency

Found: 17 | Differences: 5

Heparin cofactor 2 deficiency and Von Willebrand's disease sharing 12 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Bleeding/excessive from mild trauma
Bruising/Ecchymosis
Petechiae/Petechial rash
Purpura
Bleeding in first trimester
Bleeding in pregnancy
Bleeding in third trimester
Excessive/easy bruising tendency
Glove stool exam guaiac positive
Rectal bleeding, gross red
Rectal Blood/Bleeding
Stool color/appearance abnormal
Bleeding from Mouth in Elderly
Bleeding from mouth/oral blood
Bleeding gums
Bleeding/prolonged dental surgery
Blood in mouth/gums/throat
Flooding menstrual bleeding
Metamenorrhagia
Uterine Bleeding
Vaginal Bleeding
Vaginal bleeding/child
Vaginal Bleeding/First Trimester
Vaginal Bleeding/Pregnancy
Epistaxis Children
Epistaxis, severe/persistent
Hematuria, gross
Typical Clinical Presentation
Females sicker than males/characteristic
Presentation/Hereditary bleeder/normal labs
Clinical Presentation & Variations
Presentation/GI Bleeding Recurrent No obvious source
Presentation/Adolescent Female Flooding Periods Anemic
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Past History
Past History/GI Bleeding
Population Group
Child
Infant
Population/Pediatrics population
Woman
Young Adult
Family History
Family history/Bleeding disorders
Family history/Blood disease
Sex & Age Groups
Population/Adult/all
Population/Child
Population/Children/all
Population/Female
Population/Girl patient
Population/Infant
Population/Infant female
Population/Woman patient
Population/Young adult
Laboratory Tests
Abnormal Lab Findings (Non Measured)
Bleeding time prolonged/platelet count normal (Lab)
Clotting factor assay/abnormal (Lab)
Factor VIII Binding Assay Abnormal
PFA100 (Platelet Function Assay/?) abnormal
Platelet clumping failure on finger stick (Lab)
Platelets Adhesion defective/Normal aggregation (Lab)
PTT increased normal PT (Lab)
Ristocetin/platelet aggregation abnormal (Lab)
Transient thrombocytopenia (Lab)
VonWillebrand antigen/activity abnormal (Lab)
Fecal Globin Immunochemical Test positive
Abnormal Lab Findings - Decreased
Factor 13 (Lab)
Factor 8 (Lab)
Prothrombin consumption (Lab)
Von Willebrand factor (Lab)
Abnormal Lab Findings - Increased
Bleeding time, Duke (Lab)
Clotting time/Activated clotting time test (Lab)
PTT/Partial Thromboplastin Time/Activated PTT (Lab)
Thromboplastin generation time (Lab)
STOOL Occult blood
Diagnostic Test Results
Other Tests & Procedures
TEST/Tourniquet test abnormal
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Purpura, idiopathic thrombocytopenic
Telangiectasia,hereditary hemorrhagic
Associated Disease & Complications - Causes
Bleeding complications/Surgery
Bleeding diathesis/hemorrhagic diathesis
Bleeding Tendency
Epistaxis/nosebleed
Gastrointestinal bleeding
Hemarthrosis
Hemophilic arthritis
Hemothorax
Intracerebral hematoma
Iron deficiency anemia
Menorrhagia
Muscle Hematoma
Peripheral neuropathy
Platelet manifestation/defect
Polyneuritis
Postpartum hemorrhage
Puerperal hemorrhage/tears/lacerations
Recurrent GI Bleeding
Subdural hematoma
Von Willebrands disease
Lower GI bleeding
Recurrent GI bleed/elderly/no real source
Polyneuropathy
Disease Synergy
Synergy/Aspirin drug
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Capillary/microcirculation disorder (ex)
CLASS/Hematologic (category)
CLASS/Platelet disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 12p13
Pathophysiology/Gene locus 12p13.3
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary disease/Adult manifestations
Pathophysiology/Platelet amplification activation defect
Pathophysiology/Platelets unable to anchor to endothelium
Pathophysiology/Proteins/blood disorder (ex)
Pathophysiology/Vascular integrity/deficiency Factor 8
Pathophysiology/Von Willebrand factor deficiency
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Eponymic (category)
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Variant expressions/Subsets (ex)
PROCESS/Coagulation derangement/disorder (ex)
PROCESS/Hereditary hemorrhagic/coagulation disorder (ex)
Synonyms
Synonym
Synonym/Angiohemophilia
Synonym/Pseudohemophilia
Synonym/Thrombopathy, constitutional
Synonym/Vascular hemophilia
Synonym/Willebrand-Juergens disease
Treatment
Drug Therapy - Contraindication
RX/Aspirin (Acetylsalicylic acid)
Drug Therapy - Indication
RX/Cryoprecipitate
RX/Desmopressin (DDAVP)
RX/Oral contraceptive
RX/Progestins medication
Clinical Manifestations
Disease Progression
Course/Chronic disorder
Course/Chronic only
Demographics & Risk Factors
Population Group
Child
Population/Pediatrics population
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Associated Diseases & Rule outs
Associated Disease & Complications
Migratory superficial phlebitis
Disease Mechanism & Classification
Class
CLASS/Hematologic (category)
Pathophysiology
Pathophysiology/Gene locus 22q11
Pathophysiology/Gene locus Chromosome 22q
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process
PROCESS/Enzyme defect/Metabolic disorder (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Metabolic/storage disorder (category)
PROCESS/Coagulation derangement/disorder (ex)
PROCESS/Hereditary hypercoagulation/thrombosis disorders (ex)
Ads