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THPH1
MCID: THR092
MIFTS: 74

Thrombophilia Due to Thrombin Defect (THPH1)

Categories: Blood diseases, Bone diseases, Cardiovascular diseases, Genetic diseases, Immune diseases, Rare diseases, Respiratory diseases
Genes Variations Tissues Related diseases Publications Pathways Symptoms & Phenotypes Drugs
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Aliases & Classifications for Thrombophilia Due to Thrombin Defect

About this section

MalaCards integrated aliases for Thrombophilia Due to Thrombin Defect:

Name: Thrombophilia Due to Thrombin Defect 57 12 73 29 13 6 15
Venous Thromboembolism 57 73 6 17 71
Thrombophilia Due to Factor 2 Defect 57 12 20 73
Venous Thrombosis 57 73 54 71
Thromboembolism 57 54 6 71
Venous Thromboembolism, Susceptibility to 57 29 6
Thph1 57 12 73
Venous Thrombosis, Protection Against 57 6
Venous Thrombosis, Susceptibility to 29 6
Thromboembolism, Susceptibility to 57 29
Prothrombin-Related Thrombophilia 12 20
Thrombophilia,due to Thrombin Defect 39
Prothrombin 20210g>a Thrombophilia 20
Prothrombin G20210a Thrombophilia 20
Factor Ii-Related Thrombophilia 20
Prothrombin Thrombophilia 20
F2-Related Thrombophilia 20
Hyperprothrombinemia 20

Characteristics:

OMIM®:

57 (Updated 05-Mar-2021)
Inheritance:
autosomal dominant

Miscellaneous:
onset in childhood


HPO:

31
thrombophilia due to thrombin defect:
Inheritance autosomal dominant inheritance
Onset and clinical course childhood onset


Classifications:

MalaCards categories:
Global: Genetic diseases Rare diseases
Anatomical: Blood diseases Immune diseases Bone diseases Respiratory diseases Cardiovascular diseases
See all MalaCards categories (disease lists)


External Ids:

Disease Ontology 12 DOID:0111907
OMIM® 57 188050
OMIM Phenotypic Series 57 PS188050
MeSH 44 D019851
UMLS 71 C0040038 C0042487 C1861172 more
Sources

Summaries for Thrombophilia Due to Thrombin Defect

About this section
GARD : 20 Prothrombin-related thrombophilia affects the way the blood clots. Individuals who have a thrombophilia have an increased risk to form abnormal blood clots in blood vessels. Symptoms of prothrombin-related thrombophilia include a higher than average risk to develop blood clots in the deep veins of the legs (deep venous thrombosis) and blood clots in the lungs (pulmonary embolism). Many people with prothrombin-related thrombophilia never develop abnormal blood clots. This condition is caused by a particular genetic variant (written G20210A or 20210G>A) in the F2 gene and is inherited in an autosomal dominant pattern. Prothrombin-related thrombophilia is diagnosed based on the symptoms, physical exam, blood tests, and imaging studies. The diagnosis may be confirmed by the results of genetic testing. Treatment is focused on preventing blood clots and may include blood thinning medications.

MalaCards based summary : Thrombophilia Due to Thrombin Defect, also known as venous thromboembolism, is related to may-thurner syndrome and prothrombin thrombophilia. An important gene associated with Thrombophilia Due to Thrombin Defect is F2 (Coagulation Factor II, Thrombin), and among its related pathways/superpathways are Collagen chain trimerization and Response to elevated platelet cytosolic Ca2+. The drugs Atorvastatin and Estradiol have been mentioned in the context of this disorder. Affiliated tissues include lung, brain and liver, and related phenotypes are pulmonary embolism and deep venous thrombosis

Disease Ontology : 12 A thrombophilia characterized by recurrent thrombophilia that has material basis in heterozygous mutation in F2 on chromosome 11p11.2.

OMIM® : 57 Thrombophilia is a multifactorial disorder of inappropriate clot formation resulting from an interaction of genetic, acquired, and circumstantial predisposing factors. Venous thromboembolism most commonly manifests as deep vein thrombosis, which may progress to pulmonary embolism if the clot dislodges and travels to the lung. Other manifestations include thromboses of the cerebral or visceral veins and recurrent pregnancy loss (summary by Seligsohn and Lubetsky, 2001 and Varga and Kujovich, 2012). (188050) (Updated 05-Mar-2021)

UniProtKB/Swiss-Prot : 73 Thrombophilia due to thrombin defect: A multifactorial disorder of hemostasis characterized by abnormal platelet aggregation in response to various agents and recurrent thrombi formation.

Sources

Related Diseases for Thrombophilia Due to Thrombin Defect

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Diseases in the Thrombophilia family:

Thrombophilia Due to Thrombin Defect Thrombophilia Due to Activated Protein C Resistance
Thrombophilia, Familial, Due to Decreased Release of Tissue Plasminogen Activator Thrombophilia Due to Thrombomodulin Defect
Thrombophilia Due to Decreased Release of Plat Rare Hereditary Thrombophilia

Diseases related to Thrombophilia Due to Thrombin Defect via text searches within MalaCards or GeneCards Suite gene sharing:

(show top 50) (show all 1400)
# Related Disease Score Top Affiliating Genes
1 may-thurner syndrome 32.3 F5 APOH
2 prothrombin thrombophilia 32.1 MTHFR HABP2 F2 F13A1
3 post-thrombotic syndrome 31.7 SERPINE1 SERPINC1 F8 F5 F3 F2
4 homocysteinemia 31.4 THBD SERPINE1 SERPINC1 MTHFR F5 F2
5 protein c deficiency 31.2 THBD SERPINE1 SERPINC1 PROC MTHFR F5
6 papilledema 31.1 SERPINC1 F3 F2 APOH
7 thoracic outlet syndrome 31.1 SERPINC1 F2
8 intracranial hypotension 31.1 SERPINC1 F3 F2
9 venous insufficiency 31.1 SERPINE1 PLAT MTHFR F5 F2
10 protein s deficiency 31.0 THBD SERPINC1 PROC MTHFR FGA F5
11 mastoiditis 30.9 SERPINC1 MTHFR F2
12 chronic venous insufficiency 30.9 SERPINE1 PLAT MTHFR F2
13 cerebral sinovenous thrombosis 30.9 MTHFR F5 F3 F2 APOH
14 lateral sinus thrombosis 30.9 SERPINC1 MTHFR F2
15 hemoglobinuria 30.9 THBD SERPINC1 F2
16 varicose veins 30.9 THBD SERPINC1 PLAT MTHFR F5 F2
17 paroxysmal nocturnal hemoglobinuria 30.8 THBD SERPINC1 F2
18 intracranial hypertension 30.8 SERPINE1 SERPINC1 MTHFR F5 F3 F2
19 sagittal sinus thrombosis 30.8 SERPINC1 F8 F5 F3 F2
20 lemierre's syndrome 30.8 MTHFR F3 F2
21 cardiovascular system disease 30.8 THBD SERPINE1 SERPINC1 PLAT PF4 MTHFR
22 esophageal varix 30.7 SERPINC1 F3 F2
23 heparin-induced thrombocytopenia 30.7 SERPINC1 PF4 F3 F10
24 budd-chiari syndrome 30.7 SERPINC1 MTHFR F5 F3 F2 APOH
25 compartment syndrome 30.7 SERPINC1 F8 F3 F2
26 cavernous sinus thrombosis 30.7 SERPINC1 F3 F2
27 thrombophilia due to activated protein c resistance 30.6 THBD SERPINE1 SERPINC1 MTHFR F8 F5
28 sudden sensorineural hearing loss 30.5 MTHFR F5 F2
29 factor xii deficiency 30.5 SERPINC1 F5 F3 APOH
30 polycythemia vera 30.5 THBD PF4 F5 F2
31 thrombocytosis 30.5 SERPINC1 PF4 FGA F3 F2
32 splenic infarction 30.5 SERPINC1 F3 F2 APOH
33 limb ischemia 30.5 SERPINE1 PLAT F2
34 homocystinuria 30.5 THBD SERPINC1 MTHFR F8 F5
35 eclampsia 30.5 THBD SERPINC1 MTHFR F2
36 pregnancy loss, recurrent 1 30.4 F5 APOH
37 active peptic ulcer disease 30.4 F3 F2
38 acquired hemophilia a 30.4 F8 F5 F3
39 sticky platelet syndrome 30.4 SERPINE1 SERPINC1 F5
40 thrombotic microangiopathy 30.4 THBD F3
41 portal vein thrombosis 30.3 SERPINE1 SERPINC1 PROC PLAT MTHFR F5
42 atherosclerosis susceptibility 30.3 THBD SERPINE1 MTHFR F3
43 thrombasthenia 30.3 MTHFR F5 F3 F2
44 inflammatory bowel disease 30.3 SERPINC1 PROCR MTHFR F5 F3 F2
45 severe pre-eclampsia 30.3 SERPINC1 F5 APOH
46 intracranial embolism 30.3 SERPINC1 PLAT F3 F2
47 hemolytic anemia 30.3 THBD F3 F2 APOH
48 respiratory failure 30.3 THBD PF4 FGA F3 F2
49 antithrombin iii deficiency 30.3 SERPINC1 PF4 MTHFR FGA F5 F2
50 mitral valve stenosis 30.3 SERPINC1 PF4 FGA F3 F2

Comorbidity relations with Thrombophilia Due to Thrombin Defect via Phenotypic Disease Network (PDN): (show all 13)


Active Peptic Ulcer Disease Acute Cystitis
Decubitus Ulcer Deficiency Anemia
Familial Atrial Fibrillation Femoral Vein Thrombophlebitis
Heart Disease Hypertension, Essential
Hypothyroidism Osteoporosis
Peripheral Vascular Disease Protein-Energy Malnutrition
Schizophreniform Disorder

Graphical network of the top 20 diseases related to Thrombophilia Due to Thrombin Defect:



Diseases related to Thrombophilia Due to Thrombin Defect
Sources

Symptoms & Phenotypes for Thrombophilia Due to Thrombin Defect

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Human phenotypes related to Thrombophilia Due to Thrombin Defect:

31
# Description HPO Frequency HPO Source Accession
1 pulmonary embolism 31 HP:0002204
2 deep venous thrombosis 31 HP:0002625
3 thromboembolism 31 HP:0001907
4 cerebral venous thrombosis 31 HP:0005305
5 recurrent thrombophlebitis 31 HP:0004419

Symptoms via clinical synopsis from OMIM®:

57 (Updated 05-Mar-2021)
Respiratory Lung:
pulmonary embolism

Neurologic Central Nervous System:
cerebral thrombosis

Cardiovascular Vascular:
deep vein thrombosis
thrombosis, recurrent

Clinical features from OMIM®:

188050 (Updated 05-Mar-2021)

MGI Mouse Phenotypes related to Thrombophilia Due to Thrombin Defect:

46
# Description MGI Source Accession Score Top Affiliating Genes
1 homeostasis/metabolism MP:0005376 10.36 APOH F10 F13A1 F13B F2 F3
2 cardiovascular system MP:0005385 10.27 F10 F13A1 F2 F3 F5 FGA
3 hematopoietic system MP:0005397 10.17 F13A1 F3 F8 FGA PF4 PLAT
4 immune system MP:0005387 10.11 F2 F3 F8 FGA HABP2 PLAT
5 mortality/aging MP:0010768 10.09 APOH F10 F13A1 F2 F3 F5
6 integument MP:0010771 10.02 F13A1 F2 F3 F5 FGA MTHFR
7 liver/biliary system MP:0005370 9.86 F5 FGA HABP2 MTHFR PROC SERPINC1
8 reproductive system MP:0005389 9.61 F10 F13A1 F2 F8 FGA MTHFR
9 respiratory system MP:0005388 9.17 F13A1 F2 F3 PLAT PROC SERPINE1
Sources

Drugs & Therapeutics for Thrombophilia Due to Thrombin Defect

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Drugs for Thrombophilia Due to Thrombin Defect (from DrugBank, HMDB, Dgidb, PharmGKB, IUPHAR, NovoSeek, BitterDB):

(show top 50) (show all 342)
# Name Status Phase Clinical Trials Cas Number PubChem Id
1
Atorvastatin Approved Phase 4 134523-00-5 60823
2
Estradiol Approved, Investigational, Vet_approved Phase 4 50-28-2 5757
3
Norethindrone Approved Phase 4 68-22-4 6230
4
Polyestradiol phosphate Approved Phase 4 28014-46-2
5
Tranylcypromine Approved, Investigational Phase 4 155-09-9 441233
6
Nadroparin Approved, Investigational Phase 4
7
Clotrimazole Approved, Vet_approved Phase 4 23593-75-1 2812
8
Miconazole Approved, Investigational, Vet_approved Phase 4 22916-47-8 4189
9 fluindione Approved, Investigational Phase 4 957-56-2
10
Acetaminophen Approved Phase 4 103-90-2 1983
11
Phenindione Approved, Investigational Phase 4 83-12-5 4760
12
Amoxicillin Approved, Vet_approved Phase 4 26787-78-0 33613
13
Clavulanate Approved, Vet_approved Phase 4 58001-44-8 5280980
14
Salicylic acid Approved, Investigational, Vet_approved Phase 4 69-72-7 338
15
Streptokinase Approved, Investigational Phase 4 9002-01-1
16
Dipyridamole Approved Phase 4 58-32-2 3108
17
Ketoconazole Approved, Investigational Phase 4 65277-42-1 47576
18
Dronedarone Approved Phase 4 141626-36-0, 141625-93-6 154087
19
Rabeprazole Approved, Investigational Phase 4 117976-89-3 5029
20
Verapamil Approved Phase 4 52-53-9 2520
21
Vitamin K1 Approved, Investigational Phase 4 84-80-0 5284607
22
Dalteparin Approved Phase 4 9005-49-6
23
Tinzaparin Approved Phase 4 9041-08-1, 9005-49-6 25244225
24
Apixaban Approved Phase 4 503612-47-3 10182969
25
Phenprocoumon Approved, Investigational Phase 4 435-97-2 9908 54680692
26
Ranibizumab Approved Phase 4 347396-82-1 459903
27
Vitamin A Approved, Nutraceutical, Vet_approved Phase 4 68-26-8, 11103-57-4 445354
28
Menadione Approved, Nutraceutical Phase 4 58-27-5 4055
29
Coumarin Experimental Phase 4 91-64-5 323
30 Menaquinone Investigational Phase 4 1182-68-9
31 Contraceptive Agents Phase 4
32 Estradiol 17 beta-cypionate Phase 4
33 Estradiol 3-benzoate Phase 4
34 Estrogens Phase 4
35 Norethindrone Acetate Phase 4
36 Psychotropic Drugs Phase 4
37 Antidepressive Agents Phase 4
38 Anti-Anxiety Agents Phase 4
39 Monoamine Oxidase Inhibitors Phase 4
40
Terephthalic acid Phase 4 100-21-0 7489
41 Calcium, Dietary Phase 4
42 Antifungal Agents Phase 4
43 Tin Fluorides Phase 4
44 Dermatologic Agents Phase 4
45 Vasoconstrictor Agents Phase 4
46 Antibodies, Antiphospholipid Phase 4
47 Antivitamins K Phase 4
48 Amoxicillin-Potassium Clavulanate Combination Phase 4
49 beta-Lactamase Inhibitors Phase 4
50 Keratolytic Agents Phase 4

Interventional clinical trials:

(show top 50) (show all 1337)
# Name Status NCT ID Phase Drugs
1 The Danish Non-vitamin K Antagonist Oral Anticoagulation Study. A Cluster Randomized Study Comparing Safety and Efficacy of Edoxaban, Apixaban, Rivaroxaban and Dabigatran for Oral Anticoagulation in Patients With Venous Thromboembolism. Unknown status NCT03129555 Phase 4 Dabigatran Etexilate Oral Capsule;Rivaroxaban Oral Tablet;Edoxaban Oral Tablet;Apixaban Oral Tablet
2 Comparison of Topical Tranexamic Acid and Floseal® on Blood Loss After Total Knee Arthroplasty in Patients With a Thromboembolic Risk Unknown status NCT02865174 Phase 4 Topical tranexamic acid;Floseal®;Enoxaparin
3 Weight Based Enoxaparin for Venous Thromboembolism Prophylaxis in Trauma Patients Unknown status NCT01916707 Phase 4 Dosing of enoxaparin for VTE prophylaxis
4 A Double-blind Randomized Trial to Compare the Efficacy of Intermittent Pneumatic Compression (IPC) With and Without Early Anticoagulant Treatment for Prevention of Venous Thromboembolism (VTE) in Patients With Acute Primary Intracerebral Hemorrhage (ICH) Unknown status NCT00699465 Phase 4 enoxaparin;enoxaparin placebo
5 Evaluation of Venous Thromboembolism Prevention in High-Risk Trauma Patients: A Prospective Randomized Trial of Standard Enoxaparin Versus Two Anti-Xa Adjusted Dosing Strategies Unknown status NCT02412982 Phase 4 Enoxaparin 40 mg q12h;Enoxaparin 30 mg q8h
6 A Randomized Study Aimed at Comparing Activated Partial Thromboplastin Time and Anti-Xa Activity and in Patients Requiring Unfractionated Heparin Infusion Unknown status NCT03426982 Phase 4 Unfractionated heparin;Unfractionated heparin
7 Two Weeks of Low Molecular Weight Heparin for Distal Vein Thrombosis (TWISTER) Unknown status NCT01252420 Phase 4 Enoxaparin
8 Outcome of Percutaneous Mechanical Thrombectomy to Treat Acute Deep Venous Thrombosis Unknown status NCT02959801 Phase 4
9 Comparison of Ultra-low-dose Oral Versus Trans-dermal Hormone Therapy on Coagulation Activation and Metabolic Risk Factors for Cardiovascular Disease Unknown status NCT02264743 Phase 4 Femoston Conti;EVOREL® CONTI
10 Residual Vein Thrombosis Establishes the Optimal Duration of Low Molecular Weight Heparins in Cancer Patients With Deep Vein Thrombosis of the Lower Limbs Unknown status NCT00450645 Phase 4 low molecular weight heparin
11 Reload of High Dose Atorvastatin for Preventing Deep Vein Thrombosis in Statin Users Undergoing Total Knee Replacement Arthroplasty: RE-STOP-DVT Study- A Prospective Randomized Controlled Trial Unknown status NCT01063426 Phase 4 High dose Atorvastatin+enoxaparin;Enoxaparin
12 Rosuvastatin for Prevention of Deep Vein Thrombosis in Patients Undergoing Total Knee Replacement Arthroplasty: STOP DVT - A Prospective Randomized Controlled Trial Unknown status NCT01021488 Phase 4 Rosuvastatin 20mg/d for 14days;enoxaparin only
13 Effect of Anticoagulation After Endoscopic Therapy in Cirrhotic Patients With Portal Vein Thrombosis：A Zelen-design Multicenter Randomized Controlled Trial Unknown status NCT02630095 Phase 4 Nadroparin Calcium and Warfarin
14 Study of the OmniWave Endovascular System in Subjects With Lower and Upper Extremity Deep Vein Thrombosis - SONIC I Study Unknown status NCT00640731 Phase 4
15 A Zelen-design Randomized Controlled Trial of the Effect of Anticoagulation After Endoscopic Therapy in Cirrhotic Patients With Portal Vein Thrombosis Unknown status NCT02398357 Phase 4 Nadroparin Calcium and Warfarin
16 A Prospective Randomized Controlled Trial of Efficacy and Safety of Anticoagulant Therapy With Low Molecular Weight Heparin and Warfarin in Portal Vein Thrombosis of Liver Cirrhosis Unknown status NCT04173429 Phase 4 Low molecular weight heparin (LMWH), warfarin
17 Efficacy and Safety of Warfarin Anticoagulation for Prevention of Portal Vein Thrombosis in Liver Cirrhotic Patients With Hypersplenism After Laparoscopic Splenectomy Unknown status NCT02238444 Phase 4 Warfarin;Dipyridamole;Aspirin;Low Molecular Weight Heparin
18 Dose Effect of Tranexamic Acid on the Incidence of Deep Venous Thrombus in Cardiac Surgery With Cardiopulmonary Bypass Unknown status NCT03838328 Phase 4 Tranexamic Acid
19 Applying Pharmacogenetics to Warfarin Dosing in Chinese Patients Unknown status NCT01610141 Phase 4
20 MGuard vs bAre-metal Stents Plus Manual Thrombectomy in Real World STEMI Patients: a Prospective Multicenter Randomized Trial Unknown status NCT01124942 Phase 4
21 Thromboprophylaxis During Bariatric Surgery Unknown status NCT00444652 Phase 4 Enoxaparin
22 Comparison of Low-Molecular-Weight Heparin (LMWH) and Unfractionated Heparin (UFH) in Combination With Thrombolytic Treatment of Acute Massive Pulmonary Thromboembolism Unknown status NCT01956955 Phase 4 enoxaparin ,alteplase, unfractionated heparin
23 Low Dose Rt-PA Plus LMWH Compared With LMWH Alone for the Treatment of Normotensive Pulmonary Embolism Patients With Acute RV Dysfunction: A Randomized，Multi-Center，Controlled Trial Unknown status NCT01531829 Phase 4 Recombinant tissue plasminogen activator (rt-PA);Low Molecular Weight Heparin
24 Prospective, Pharmacokinetic Study for Determination of the Relationship Between Lean Body Weight and Anti-Xa Activity 4 Hours After Subcutaneous Injection of 5700 IU Nadroparin in Morbidly Obese Patients After Bariatric Surgery. Unknown status NCT02295150 Phase 4 Nadroparin
25 Venous Thromboembolism Prevention in the Morbidly Obese Medically Ill Patient: A Pharmacological Analysis of the Predictability of Prophylactic Weight-Based Enoxaparin Dosing. Completed NCT00585182 Phase 4 Enoxaparin 0.5 mg/kg once daily
26 A Randomized Trial of the Effect of Low-Molecular-Weight Heparin Versus Warfarin Sodium on the Mortality in the Long-Term Treatment of Proximal Deep Vein Thrombosis (Main LITE Study) Completed NCT00203580 Phase 4 Tinzaparin sodium
27 Safety of Fondaparinux as Postpartum Venous Thromboembolism Prophylaxis Completed NCT04447378 Phase 4 Fondaparinux 2.5Mg/0.5Ml Inj Syr
28 Cystic Fibrosis and Totally Implantable Vascular Access Devices: Evaluation of the Incidence of Venous Thrombosis Related to the Catheter and Study of the Genetic and Acquired Risk Factors Completed NCT00244270 Phase 4
29 PREPIC 2 : Interruption of Inferior Vena Cava by a Retrievable Filter for the Prevention of Recurrent Pulmonary Embolism : a Randomised, Open Label Study Completed NCT00457158 Phase 4
30 Efficacy and Safety of Warfarin Anticoagulation for Prevention of Portal Vein Thrombosis in Liver Cirrhotic Patients After Laparoscopic Splenectomy and Azygoportal Disconnection for Portal Hypertension Completed NCT02247414 Phase 4 Warfarin;Dipyridamole;Aspirin;Low Molecular Weight Heparin
31 Apixaban for Primary Prevention of Venous Thromboembolism in Patients With Multiple Myeloma Receiving Immunomodulatory Therapy Completed NCT02958969 Phase 4 Apixaban
32 Venous Thromboembolic Prophylaxis After Major Trauma: A Randomized Controlled Trial of Three Times a Day Unfractionated Heparin Versus Twice a Day Enoxaparin Completed NCT01729559 Phase 4 5000 Units unfractionated Heparin Q 8 hr;30mg enoxaparin Q12 hr
33 Phase IV, Randomized, Open-Label Trial Comparing Long-Term Subcutaneous Low-Molecular Weight Heparin With Oral Anticoagulant Therapy in the Treatment of Deep Venous Thrombosis Completed NCT00689520 Phase 4 tinzaparin;acenocoumarol
34 D-dimer Test to Establish Duration of Anticoagulation After a First Idiopathic Episode of Venous Thromboembolism; the Prospective Randomized "Prolong" Study Completed NCT00264277 Phase 4 Vitamin K antagonist (Coumarin anticoagulants)
35 The Efficacy of Subcutaneous Enoxaparin Once Daily in the Treatment of Acute Venous Thromboembolic Disease: an Open-labelled, Non-comparative, Multicentric, Phase IV Trial Completed NCT00265993 Phase 4 enoxaparin
36 Clinically-Important Venous Thromboembolism Following Lower Extremity Fractures: Epidemiology & Prevention Completed NCT00187408 Phase 4 Low Molecular Weight Heparin (dalteparin)
37 APB Study: Apixaban Pharmacokinetics in Bariatric Patients Completed NCT02406885 Phase 4 Apixaban
38 Reversion of the Anticoagulant Effect of the New Antithrombotic Agents Anti-Xa and Anti IIa by Specific and Non-specific Haemostatic Drugs,: an Ex-Vivo Study in Healthy Volunteers Completed NCT01210755 Phase 4 Rivaroxaban, Dabigatran;Dabigatran; Rivaroxaban
39 Use of Fondaparinux in Critically Ill Patients With Renal Failure Completed NCT01467583 Phase 4 Fondaparinux
40 Plasma Anti-FXa Concentration After Continuous Intravenous Infusion and Subcutaneous Dosing of Enoxaparin for Thromboprophylaxis in Critically Ill Patients Completed NCT02095509 Phase 4 Enoxaparin
41 EUropean Pharmacogenetics of AntiCoagulant Therapy - Warfarin Completed NCT01119300 Phase 4
42 EUropean Pharmacogenetics of AntiCoagulant Therapy - Phenprocoumon Completed NCT01119274 Phase 4
43 A Double-Blind, Placebo-Controlled, Parallel, Multicenter Study on Extended VTE Prophylaxis in Acutely Ill Medical Patients With Prolonged Immobilization Completed NCT00077753 Phase 4 enoxaparin sodium
44 Spreading and Improving DVT Prophylaxis at Mayo Clinic (DVT-P-Spread) Completed NCT01304108 Phase 4
45 EUropean Pharmacogenetics of AntiCoagulant Therapy - Acenocoumarol Completed NCT01119261 Phase 4
46 Comparison of Bleeding Risk Between Rivaroxaban and Apixaban for the Treatment of Acute Venous Thromboembolism: The Pilot Study Completed NCT02559856 Phase 4 Apixaban;Rivaroxaban
47 Evaluation of Non-Surgical Venous Thromboembolism Prophylaxis Dosing Strategies: Enoxaparin 20mg Versus 30mg Subcutaneously Once Daily in Elderly Patients With Impaired Renal Function Completed NCT03158792 Phase 4 Enoxaparin 20Mg/0.2mL Prefilled Syringe;Enoxaparin 60Mg/0.6Ml Inj Syringe 0.6Ml
48 REVERSEII: Validation of the "Men and HERDOO2"- A Clinical Decision Rule to Identify Patients With "Unprovoked" Venous Thromboembolism Who Can Discontinue Anticoagulants After 6 Months of Treatment. Completed NCT00967304 Phase 4
49 Weight-Adjusted Dosing of Tinzaparin in Pregnancy Completed NCT00851864 Phase 4 Tinzaparin
50 Prospective, Multicenter Study Investigating Efficacy and Safety of Oral Rivaroxaban for the Prevention of Recurrent Venous Thromboembolism in Korean Patients With Cancers Completed NCT01989845 Phase 4 Rivaroxaban

Search NIH Clinical Center for Thrombophilia Due to Thrombin Defect

Inferred drug relations via UMLS 71 / NDF-RT 51 :


anisindione
apixaban
ardeparin
ardeparin sodium
argatroban
Dalteparin
Dalteparin Sodium
danaparoid
Danaparoid sodium
Dicumarol
Enoxaparin
fondaparinux
heparin
heparin calcium
heparin sodium
HEPARIN SODIUM (BEEF LUNG)
heparin sodium, bovine
heparin sodium, porcine
lepirudin
Papaverine
Papaverine Hydrochloride
Phenprocoumon
rivaroxaban
Streptokinase
tinzaparin
Tinzaparin sodium
Urokinase
Warfarin
Warfarin Sodium
WARFARIN SODIUM ISOPROPANOL COMPLEX
Sources

Genetic Tests for Thrombophilia Due to Thrombin Defect

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Genetic tests related to Thrombophilia Due to Thrombin Defect:

# Genetic test Affiliating Genes
1 Thrombophilia Due to Thrombin Defect 29 F13A1 F2 HABP2 MTHFR
2 Venous Thrombosis, Susceptibility to 29
3 Venous Thromboembolism, Susceptibility to 29
4 Thromboembolism, Susceptibility to 29
Sources

Anatomical Context for Thrombophilia Due to Thrombin Defect

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MalaCards organs/tissues related to Thrombophilia Due to Thrombin Defect:

40
Lung, Brain, Liver, Heart, Breast, Endothelial, Spinal Cord
Sources

Publications for Thrombophilia Due to Thrombin Defect

About this section

Articles related to Thrombophilia Due to Thrombin Defect:

(show top 50) (show all 22150)
# Title Authors PMID Year
1
The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation. 54 57 6
10477778 1999
2
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. 54 57 6
8916933 1996
3
Thrombosis from a prothrombin mutation conveying antithrombin resistance. 6 57
22716977 2012
4
Clinical and analytical relevance of the combination of prothrombin 20210A/A and factor V Leiden: results from a large family. 57 6
10233438 1999
5
Frequent factor II G20210A mutation in idiopathic portal vein thrombosis. 57 6
9869612 1999
6
Marburg I polymorphism of factor VII-activating protease is associated with idiopathic venous thromboembolism. 61 6 54
15486068 2005
7
Management of inherited thrombophilia: guide for genetics professionals. 61 57
21707594 2012
8
Predictive value of factor V Leiden and prothrombin G20210A in adults with venous thromboembolism and in family members of those with a mutation: a systematic review. 6 61
19531787 2009
9
Functional polymorphisms of FGA, encoding alpha fibrinogen, are associated with susceptibility to venous thromboembolism in a Taiwanese population. 6 61
16362348 2006
10
alpha-fibrinogen Thr312Ala polymorphism and venous thromboembolism. 6 61
10910940 2000
11
Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism. 61 6
10406905 1999
12
A comparison of three months of anticoagulation with extended anticoagulation for a first episode of idiopathic venous thromboembolism. 57 61
10089183 1999
13
A single genetic origin for the common prothrombotic G20210A polymorphism in the prothrombin gene. 61 6
9694698 1998
14
HABP2 Mutation and Nonmedullary Thyroid Cancer. 6
26581004 2015
15
HABP2 Mutation and Nonmedullary Thyroid Cancer. 6
26581003 2015
16
HABP2 Mutation and Nonmedullary Thyroid Cancer. 6
26581001 2015
17
HABP2 Mutation and Nonmedullary Thyroid Cancer. 6
26581005 2015
18
HABP2 Mutation and Nonmedullary Thyroid Cancer. 6
26581002 2015
19
Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer. 6
26222560 2015
20
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. 57
20226436 2010
21
Factor XIII Val34Leu variant and the risk of myocardial infarction: a meta-analysis. 6
17393027 2007
22
Prothrombin 20210G>A is an ancestral prothrombotic mutation that occurred in whites approximately 24,000 years ago. 6
16493002 2006
23
A novel polymorphism in the factor XIII B-subunit (His95Arg): relationship to subunit dissociation and venous thrombosis. 6
16241947 2005
24
Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. 6
15534175 2004
25
Genetic variants of coagulation factor XIII, postmenopausal estrogen therapy, and risk of nonfatal myocardial infarction. 6
12456499 2003
26
Marburg I polymorphism of factor VII--activating protease: a prominent risk predictor of carotid stenosis. 6
12578864 2003
27
The frequent Marburg I polymorphism impairs the pro-urokinase activating potency of the factor VII activating protease (FSAP). 6
12138371 2002
28
The effect of the Val34Leu polymorphism in the factor XIII gene in infants with a birth weight below 1500 g. 6
12072871 2002
29
Unilateral chronic thromboembolic pulmonary disease associated with combined inherited thrombophilia. 6
11796466 2002
30
[A family with multiple thrombosis including infancy occurrence]. 57
11570053 2001
31
Thrombophilic gene mutations and recurrent spontaneous abortion: prothrombin mutation increases the risk in the first trimester. 6
11506076 2001
32
Increased efficiency of mRNA 3' end formation: a new genetic mechanism contributing to hereditary thrombophilia. 6
11443298 2001
33
Genetic susceptibility to venous thrombosis. 57
11309638 2001
34
The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure. 6
10910914 2000
35
Budd-Chiari syndrome in a patient heterozygous for both factor V Leiden and the G20210A mutation on the prothrombin gene. 6
10544935 1999
36
The 20210A allele of the prothrombin gene is an independent risk factor for perception deafness in patients with venous thromboembolic antecedents. 6
10336270 1999
37
Factor XIII Val34Leu is a genetic factor involved in the etiology of venous thrombosis. 6
10365735 1999
38
Born to clot: the European burden. 6
10233439 1999
39
Venous thrombosis as a chronic disease. 57
10089190 1999
40
Simultaneous genotyping for factor V Leiden and prothrombin G20210A variant by a multiplex PCR-SSCP assay on whole blood. 6
10348711 1999
41
The 20210 G-->A mutation in the 3'-untranslated region of the prothrombin gene and the risk for arterial thrombotic disease. 6
10027711 1999
42
The prevalence of the prothrombin 20210 G-->A mutation is not increased in angiographically confirmed coronary artery disease. 6
10348710 1999
43
The 20210 G to A prothrombin polymorphism and late complications in type 1 diabetes mellitus. 6
10348712 1999
44
Factor XIII Val 34 Leu: a novel association with primary intracerebral hemorrhage. 6
9550516 1998
45
Geographic distribution of the 20210 G to A prothrombin variant. 6
9569177 1998
46
Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A. 6
9531249 1998
47
Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene. 6
9493607 1998
48
Association of a common polymorphism in the factor XIII gene with myocardial infarction. 6
9459313 1998
49
A common prothrombin variant (20210 G to A) increases the risk of myocardial infarction in young women. 6
9292507 1997
50
Deficiency in the A-subunit of coagulation factor XIII: two novel point mutations demonstrate different effects on transcript levels. 6
8025280 1994
Sources

Variations for Thrombophilia Due to Thrombin Defect

About this section

ClinVar genetic disease variations for Thrombophilia Due to Thrombin Defect:

6 (show top 50) (show all 263)
# Gene Name Type Significance ClinVarId dbSNP ID GRCh37 Pos GRCh38 Pos
1 F13A1 NM_000129.3(F13A1):c.103G>T (p.Val35Leu) SNV protective 16532 rs5985 6:6318795-6318795 6:6318562-6318562
2 PLOD1 GRCh37/hg19 1p36.22(chr1:12019879-12028775) copy number gain Pathogenic 523241 1:12019879-12028775
3 F2 NM_000506.5(F2):c.1787G>A (p.Arg596Gln) SNV Pathogenic 692073 rs387907201 11:46760876-46760876 11:46739326-46739326
4 F2 NM_000506.5(F2):c.*97G>A SNV Pathogenic 13310 rs1799963 11:46761055-46761055 11:46739505-46739505
5 F13B NM_001994.2(F13B):c.344G>A (p.Arg115His) SNV risk factor 16520 rs6003 1:197031021-197031021 1:197061891-197061891
6 PROC NM_000312.3(PROC):c.352T>C (p.Phe118Leu) SNV Likely pathogenic 469122 rs1553424043 2:128180699-128180699 2:127423123-127423123
7 PROC NM_000312.3(PROC):c.125G>A (p.Arg42His) SNV Likely pathogenic 161333 rs369504169 2:128178913-128178913 2:127421337-127421337
8 PROC NM_000312.3(PROC):c.814C>T (p.Arg272Cys) SNV Likely pathogenic 671 rs121918154 2:128185950-128185950 2:127428374-127428374
9 PROC NM_000312.3(PROC):c.238-2A>G SNV Likely pathogenic 627040 rs1573442055 2:128180491-128180491 2:127422915-127422915
10 HABP2 NM_004132.5(HABP2):c.1601G>A (p.Gly534Glu) SNV risk factor 5974 rs7080536 10:115348046-115348046 10:113588287-113588287
11 FGA NM_021871.4(FGA):c.991A>G (p.Thr331Ala) SNV risk factor 16420 rs6050 4:155507590-155507590 4:154586438-154586438
12 F2 NM_000506.5(F2):c.*97G>A SNV risk factor 13310 rs1799963 11:46761055-46761055 11:46739505-46739505
13 F2 NM_000506.4(F2):c.1787G>T (p.Arg596Leu) SNV Conflicting interpretations of pathogenicity 31922 rs387907201 11:46760876-46760876 11:46739326-46739326
14 F5 NM_000130.5(F5):c.1158A>G (p.Gln386=) SNV Uncertain significance 876513 1:169521933-169521933 1:169552695-169552695
15 F5 NM_000130.4(F5):c.4309A>T (p.Thr1437Ser) SNV Uncertain significance 293598 rs115148599 1:169510019-169510019 1:169540781-169540781
16 F5 NM_000130.4(F5):c.6629A>T (p.Gln2210Leu) SNV Uncertain significance 293571 rs886045541 1:169483597-169483597 1:169514359-169514359
17 F5 NM_000130.4(F5):c.1545C>T (p.Ile515=) SNV Uncertain significance 293627 rs886045551 1:169519105-169519105 1:169549867-169549867
18 F5 NM_000130.4(F5):c.*216T>A SNV Uncertain significance 293567 rs186962725 1:169483335-169483335 1:169514097-169514097
19 F5 NM_000130.4(F5):c.3307A>T (p.Asn1103Tyr) SNV Uncertain significance 293611 rs886045548 1:169511021-169511021 1:169541783-169541783
20 F5 NM_000130.4(F5):c.*891A>G SNV Uncertain significance 293555 rs9332674 1:169482660-169482660 1:169513422-169513422
21 F5 NM_000130.4(F5):c.111T>A (p.Ala37=) SNV Uncertain significance 293643 rs537081933 1:169555514-169555514 1:169586276-169586276
22 F5 NM_000130.4(F5):c.*396C>A SNV Uncertain significance 293564 rs181328696 1:169483155-169483155 1:169513917-169513917
23 F5 NM_000130.4(F5):c.1391C>T (p.Thr464Ile) SNV Uncertain significance 293629 rs141768227 1:169519883-169519883 1:169550645-169550645
24 F5 NM_000130.4(F5):c.4405T>C (p.Ser1469Pro) SNV Uncertain significance 293595 rs144262027 1:169509923-169509923 1:169540685-169540685
25 F5 NM_000130.4(F5):c.6589A>G (p.Ile2197Val) SNV Uncertain significance 293572 rs372005449 1:169483637-169483637 1:169514399-169514399
26 F5 NM_000130.4(F5):c.1106C>T (p.Ala369Val) SNV Uncertain significance 293631 rs200934105 1:169524432-169524432 1:169555194-169555194
27 F5 NM_000130.4(F5):c.*1170G>A SNV Uncertain significance 293552 rs191866237 1:169482381-169482381 1:169513143-169513143
28 F5 NM_000130.4(F5):c.*157A>T SNV Uncertain significance 293568 rs886045539 1:169483394-169483394 1:169514156-169514156
29 F5 NM_000130.4(F5):c.3801T>C (p.Leu1267=) SNV Uncertain significance 293604 rs559683767 1:169510527-169510527 1:169541289-169541289
30 F5 NM_000130.4(F5):c.437G>A (p.Arg146Gln) SNV Uncertain significance 293640 rs145625079 1:169529941-169529941 1:169560703-169560703
31 F5 NM_000130.5(F5):c.5209-12_5209-11del Microsatellite Uncertain significance 293588 rs886045545 1:169499067-169499068 1:169529829-169529830
32 F5 NM_000130.4(F5):c.936C>T (p.Thr312=) SNV Uncertain significance 293633 rs758832130 1:169525900-169525900 1:169556662-169556662
33 F5 NM_000130.4(F5):c.*104A>C SNV Uncertain significance 293570 rs886045540 1:169483447-169483447 1:169514209-169514209
34 F5 NM_000130.4(F5):c.4333A>G (p.Thr1445Ala) SNV Uncertain significance 293597 rs200204656 1:169509995-169509995 1:169540757-169540757
35 F5 NM_000130.4(F5):c.4972-14A>C SNV Uncertain significance 293592 rs763080313 1:169500274-169500274 1:169531036-169531036
36 F5 NM_000130.4(F5):c.5124C>T (p.Tyr1708=) SNV Uncertain significance 293589 rs199568344 1:169500108-169500108 1:169530870-169530870
37 F5 NM_000130.4(F5):c.*441C>T SNV Uncertain significance 293562 rs188490117 1:169483110-169483110 1:169513872-169513872
38 F5 NM_000130.4(F5):c.2042A>G (p.Asp681Gly) SNV Uncertain significance 293623 rs886045550 1:169512286-169512286 1:169543048-169543048
39 F5 NM_000130.4(F5):c.2868T>C (p.Tyr956=) SNV Uncertain significance 293617 rs149067268 1:169511460-169511460 1:169542222-169542222
40 F5 NM_000130.4(F5):c.*1432C>T SNV Uncertain significance 293549 rs886045536 1:169482119-169482119 1:169512881-169512881
41 F5 NM_000130.4(F5):c.3455A>C (p.Glu1152Ala) SNV Uncertain significance 293606 rs543751483 1:169510873-169510873 1:169541635-169541635
42 F5 NM_000130.4(F5):c.*400C>G SNV Uncertain significance 293563 rs886045537 1:169483151-169483151 1:169513913-169513913
43 F5 NM_000130.4(F5):c.5721T>C (p.Cys1907=) SNV Uncertain significance 293578 rs886045543 1:169494142-169494142 1:169524904-169524904
44 F5 NM_000130.4(F5):c.*1780G>T SNV Uncertain significance 293545 rs559071301 1:169481771-169481771 1:169512533-169512533
45 F5 NM_000130.4(F5):c.5490G>A (p.Leu1830=) SNV Uncertain significance 293582 rs149092241 1:169497262-169497262 1:169528024-169528024
46 F5 NM_000130.4(F5):c.4356C>A (p.Ser1452Arg) SNV Uncertain significance 293596 rs751749207 1:169509972-169509972 1:169540734-169540734
47 F5 NM_000130.4(F5):c.*598T>G SNV Uncertain significance 293559 rs544753372 1:169482953-169482953 1:169513715-169513715
48 F5 NM_000130.4(F5):c.886G>A (p.Ala296Thr) SNV Uncertain significance 293634 rs748350385 1:169525950-169525950 1:169556712-169556712
49 F5 NM_000130.4(F5):c.6360G>A (p.Lys2120=) SNV Uncertain significance 293574 rs757104503 1:169484850-169484850 1:169515612-169515612
50 F5 NM_000130.4(F5):c.3442T>C (p.Ser1148Pro) SNV Uncertain significance 293607 rs369276714 1:169510886-169510886 1:169541648-169541648
Sources

Expression for Thrombophilia Due to Thrombin Defect

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Search GEO for disease gene expression data for Thrombophilia Due to Thrombin Defect.
Sources

Pathways for Thrombophilia Due to Thrombin Defect

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Pathways related to Thrombophilia Due to Thrombin Defect according to GeneCards Suite gene sharing:

# Super pathways Score Top Affiliating Genes
1
Collagen chain trimerization 65
Show member pathways
 12.77 THBD SERPINC1 PROC PLOD1 FGA F8
2
Response to elevated platelet cytosolic Ca2+ 65
Show member pathways
 12.6 THBD SERPINE1 SERPINC1 PROCR PROC PLAT
3
Complement and coagulation cascades 36 1
12.16 THBD SERPINE1 SERPINC1 PROCR PROC PLAT
4
Folate Metabolism 1
Show member pathways
 12.04 SERPINE1 PLAT MTHFR F2
5
Formation of Fibrin Clot (Clotting Cascade) 65
Show member pathways
 12.03 THBD SERPINE1 SERPINC1 PROCR PROC PLAT
6
Cell surface interactions at the vascular wall 65
Show member pathways
 11.97 THBD PROCR PROC PF4 F2
7
Gamma carboxylation, hypusine formation and arylsulfatase activation 65
Show member pathways
 11.69 PROC F2 F10
8
AGE-RAGE signaling pathway in diabetic complications 36
11.63 THBD SERPINE1 F3
9
Warfarin Pathway, Pharmacodynamics 60
10.72 PROC F2 F10
10
Dissolution of Fibrin Clot 65
10.55 SERPINE1 PLAT
Sources

GO Terms for Thrombophilia Due to Thrombin Defect

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Cellular components related to Thrombophilia Due to Thrombin Defect according to GeneCards Suite gene sharing:

(show all 11)
# Name GO ID Score Top Affiliating Genes
1 extracellular exosome GO:0070062 10.11 TNXA SERPINE1 SERPINC1 PROCR PLOD1 PLAT
2 extracellular region GO:0005576 10.06 SERPINE1 SERPINC1 PROCR PROC PLAT PF4
3 cell surface GO:0009986 9.91 THBD PROCR PLAT FGA F3 APOH
4 endoplasmic reticulum lumen GO:0005788 9.87 SERPINC1 PROC FGA F8 F5 F2
5 extracellular space GO:0005615 9.83 THBD SERPINE1 SERPINC1 PROCR PROC PLAT
6 platelet alpha granule lumen GO:0031093 9.73 SERPINE1 PF4 FGA F8 F5 F13A1
7 blood microparticle GO:0072562 9.71 SERPINC1 FGA F2 F13A1
8 Golgi lumen GO:0005796 9.67 PROC F2 F10
9 platelet alpha granule GO:0031091 9.48 FGA F5
10 intrinsic component of external side of plasma membrane GO:0031233 9.37 F3 F10
11 collagen-containing extracellular matrix GO:0062023 9.32 TNXA SERPINE1 SERPINC1 PLAT PF4 FGA

Biological processes related to Thrombophilia Due to Thrombin Defect according to GeneCards Suite gene sharing:

(show all 18)
# Name GO ID Score Top Affiliating Genes
1 proteolysis GO:0006508 9.97 PROC PLAT HABP2 F2 F10
2 cellular protein metabolic process GO:0044267 9.91 SERPINC1 PROC FGA F5 F2
3 ER to Golgi vesicle-mediated transport GO:0006888 9.89 PROC F8 F5 F2 F10
4 platelet activation GO:0030168 9.83 PF4 FGA F8 F2
5 hemostasis GO:0007599 9.73 THBD SERPINC1 PROCR PROC FGA F8
6 platelet degranulation GO:0002576 9.7 SERPINE1 PF4 FGA F8 F5 F13A1
7 fibrinolysis GO:0042730 9.67 SERPINE1 PLAT FGA F2
8 blood coagulation, intrinsic pathway GO:0007597 9.65 F8 F2 APOH
9 positive regulation of blood coagulation GO:0030194 9.63 SERPINE1 F2 APOH
10 negative regulation of blood coagulation GO:0030195 9.62 THBD SERPINE1 PROC APOH
11 regulation of blood coagulation GO:0030193 9.61 SERPINC1 F2 APOH
12 plasminogen activation GO:0031639 9.58 PLAT FGA APOH
13 negative regulation of platelet activation GO:0010544 9.57 THBD F2
14 negative regulation of coagulation GO:0050819 9.56 PROCR PROC
15 negative regulation of fibrinolysis GO:0051918 9.56 THBD SERPINE1 F2 APOH
16 blood coagulation, fibrin clot formation GO:0072378 9.55 FGA F13A1
17 blood coagulation, extrinsic pathway GO:0007598 9.54 F3 F10
18 blood coagulation GO:0007596 9.47 THBD SERPINC1 PROCR PROC PLAT HABP2

Molecular functions related to Thrombophilia Due to Thrombin Defect according to GeneCards Suite gene sharing:

# Name GO ID Score Top Affiliating Genes
1 peptidase activity GO:0008233 9.65 PROC PLAT HABP2 F2 F10
2 phospholipid binding GO:0005543 9.54 F3 F10 APOH
3 protease binding GO:0002020 9.5 SERPINE1 SERPINC1 F3
4 heparin binding GO:0008201 9.46 SERPINC1 PF4 F2 APOH
5 serine-type peptidase activity GO:0008236 9.35 PROC PLAT HABP2 F2 F10
6 serine-type endopeptidase activity GO:0004252 9.1 PROC PLAT HABP2 F3 F2 F10
Sources

Sources for Thrombophilia Due to Thrombin Defect

About this section
3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
20 GARD
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
53 NINDS
54 Novoseek
56 OMIM via Orphanet
57 OMIM® (Updated 05-Mar-2021)
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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