| 疾病名称 |
别名 |
|
| Pseudo-Von Willebrand Disease |
|
Bdplt3
|
Von Willebrand Disease, Platelet-Type
|
|
VWDP
|
Platelet-Type Bleeding Disorder 3
|
|
Platelet Type-Von Willebrand Disease
|
Pt-Vwd
|
|
Von Willebrand Disease Platelet-Type
|
Von Willebrand Disease, Platelet Type
|
|
Pseudo Von Willebrand Disease
|
Bleeding Disorder, Platelet-Type, 3
|
|
Pseudo-Von Willebrand Disease Type 2b
|
Bleeding Disorder Platelet-Type 3
|
|
Pseudo-Vwd
|
|
|
| Bernard-Soulier Syndrome, Type A2, Autosomal Dominant |
|
BSSA2
|
Bernard-Soulier Syndrome Type A2
|
|
Bernard-Soulier Syndrome, Type A2
|
Bernard-Soulier Syndrome A2, Autosomal Dominant
|
|
Autosomal Dominant Benign Bernard-Soulier Syndrome
|
Benign Mediterranean Macrothrombocytopenia
|
|
Bernard-Soulier Syndrome, Benign Autosomal Dominant
|
|
|
| Bernard-Soulier Syndrome |
|
Giant Platelet Syndrome
|
BSS
|
|
Von Willebrand Factor Receptor Deficiency
|
Bdplt1
|
|
Platelet Glycoprotein Ib Deficiency
|
Bernard-Soulier Syndrome, Type A1
|
|
Bernard-Soulier Syndrome, Type B
|
Bernard Soulier Syndrome
|
|
Deficiency Of Platelet Glycoprotein 1b
|
Hemorrhagiparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type C
|
Bleeding Disorder, Platelet-Type, 1
|
|
Glycoprotein Ib, Platelet, Deficiency Of
|
Giant Platelet Disorder, Isolated
|
|
Giant Platelet Disease
|
Macrothrombocytopenia, Familial Bernard-Soulier Type
|
|
Bernard-Soulier Syndrome, Type C
|
Bernard - Soulier Thrombopathy
|
|
Hemorrhagic Dystrophic Thrombocytopenia
|
Thrombopathy, Bernard-Soulier
|
|
Platelet Glycoprotein 1b, Deficiency Of
|
Hemorrhagioparous Thrombocytic Dystrophy
|
|
Bernard-Soulier Syndrome Type A1
|
Bernard-Soulier Syndrome Type B
|
|
Bleeding Disorder Platelet-Type 1
|
Gpd
|
|
Macrothrombocytopenia, Familial, Bernard-Soulier Type
|
|
|
| Nonarteritic Anterior Ischemic Optic Neuropathy |
|
Anterior Ischemic Optic Neuropathy
|
Nonarteritic Anterior Ischemic Optic Neuropathy, Susceptibility To
|
|
NAION
|
Non-Arteritic Anterior Ischemic Optic Neuropathy
|
|
Ischemic Optic Neuropathy
|
Aion
|
|
Optic Neuropathy, Ischemic
|
Naion, Susceptibility To
|
|
Optic Neuropathy, Anterior Ischemic
|
Optic Neuropathy, Anterior Ischemic, Susceptibility To
|
|
Non-Arteritic Anterior Ischaemic Optic Neuropathy
|
Nonarteritic Anterior Ischaemic Optic Neuropathy
|
|
Neuropathy, Optic, Ischemic, Nonarteritic Anterior, Susceptibility To
|
Ion - [Ischemic Optic Neuropathy]
|
|
Neuropathic Ischaemia Of N.Opticus
|
Ischaemic Neuropathy Of Optic Nerve
|
|
|
| Autosomal Dominant Macrothrombocytopenia |
|
|
| Fetal And Neonatal Alloimmune Thrombocytopenia |
|
Nait
|
Neonatal Alloimmune Thrombocytopenia
|
|
Fnait
|
|
|
| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
|
| Arteritic Anterior Ischemic Optic Neuropathy |
|
|
| Thrombosis |
|
Thrombosis Of Blood Vessel
|
|
|
| Von Willebrand'S Disease |
|
Von Willebrand Disease
|
Von Willebrand Disorder
|
|
Vascular Pseudohemophilia
|
Hereditary Von Willebrand Disease
|
|
Vwd
|
Vascular Hemophilia
|
|
Von Willebrand'S-Jurgens' Disease
|
Von Willebrand-Jrgens Disease
|
|
Von Willebrand Factor Deficiency
|
Von Willebrand Factor, Deficiency
|
|
Angiohemophilia
|
Von Willebrand'S Factor Deficiency
|
|
Von Willebrand Diseases
|
Factor Viii Deficiency With Vascular Defect
|
|
Vascular Haemophilia
|
Willebrand Jurgen Thrombopathy
|
|
Pseudohaemophilia
|
Minot-Von Willebrand-Jurgen Disease
|
|
Angiohaemophilia
|
Angiohaemophilia A
|
|
Angiohaemophilia B
|
|
|
| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
|
Thrombocytopathy
|
Platelet Dysfunction
|
|
Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
|
| Glanzmann Thrombasthenia 1 |
|
Glanzmann Thrombasthenia
|
Thrombasthenia Of Glanzmann And Naegeli
|
|
Glanzmann'S Thrombasthenia
|
Bdplt2
|
|
Platelet Glycoprotein Iib-Iiia Deficiency
|
Deficiency Of Platelet Fibrinogen Receptor
|
|
GT1
|
Gt
|
|
Platelet Fibrinogen Receptor Deficiency
|
Glycoprotein Complex Iib-Iiia Deficiency
|
|
Deficiency Of Glycoprotein Complex Iib-Iiia
|
Glycoprotein Iib/Iiia Defect
|
|
Glanzmann Thrombasthenia, Type A
|
Thrombasthenia
|
|
Bleeding Disorder, Platelet-Type, 2
|
Gp Iib-Iiia Complex Deficiency
|
|
Deficiency Of Gp Iib-Iiia Complex
|
Platelet-Type Bleeding Disorder 2
|
|
Thrombocytasthenia
|
Deficiency Of Gp 2b 3a Complex
|
|
Diacyclothrombopathia 2b 3a
|
Glanzmann Thrombasthenia Type A
|
|
Platelet Fibrinogen Receptor, Deficiency Of
|
Platelet Glycoprotein 2b 3a Deficiency
|
|
Glanzmann Disease
|
Glanzmann-Naegeli Disorder
|
|
Hereditary Hemorrhagic Thrombasthenia
|
Hereditary Thrombasthenia
|
|
Bleeding Disorder Platelet-Type 2
|
|
|
| Coronary Thrombosis |
|
Coronary Artery Thrombosis
|
|
|
| Thrombocytopenic Purpura, Autoimmune |
|
Idiopathic Thrombocytopenic Purpura
|
Autoimmune Thrombocytopenic Purpura
|
|
Immune Thrombocytopenic Purpura
|
Itp
|
|
Idiopathic Purpura
|
AITP
|
|
Ideopath Thrombocytopenic Pur
|
Primary Thrombocytopenic Purpura
|
|
Werlhof'S Disease
|
Thrombocytopenic Purpura Autoimmune
|
|
Purpura Thrombocytopenic Idiopathic
|
Purpura, Thrombocytopenic, Idiopathic
|
|
Autoimmune Thrombocytopenia
|
Thrombocytopenia Due To Platelet Alloimmunization
|
|
Idiopathic Thrombocytopenia
|
Idiopathic Thrombocytopenia Purpura
|
|
Frank'S Essential Thrombocytopenia
|
Itp - [Idiopathic Thrombocytopenia Purpura]
|
|
Werlhof Disease
|
Primary Autoimmune Thrombocytopenic Purpura
|
|
Haemorrhagic Purpura
|
Essential Thrombocytopenia
|
|
Purpura Haemorrhagica
|
|
|
| Ischemia |
|
|
| Hemorrhagic Disease |
|
Hemorrhagic Disorders
|
Hemorrhagic Diathesis
|
|
Hemorrhagic Diseases
|
Bleeding Tendency
|
|
Acquired Coagulation Factor Inhibitor Disorder
|
Acquired Inhibitor Of Coagulation
|
|
Antithrombinaemia
|
Antithromboplastinogenaemia
|
|
Circulating Anticoagulant Disorder
|
Haemorrhagic Disorder Due To Antithrombinaemia
|
|
Haemorrhagic Disorder Due To Excess Administered Heparin
|
Antithromboplastinaemia
|
|
Haemorrhagic Disorder Due To Hyperheparinemia
|
|
|
| Neuropathy |
|
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
| Bleeding Disorder, Platelet-Type, 11 |
|
BDPLT11
|
Glycoprotein Vi Deficiency
|
|
Gp Vi Deficiency
|
Platelet-Type Bleeding Disorder 11
|
|
Bleeding Diathesis Due To A Collagen Receptor Defect
|
Bleeding Diathesis Due To Glycoprotein Vi Deficiency
|
|
Platelet-Type Bleeding Disorder-11
|
Bleeding Disorder, Platelet Type 11
|
|
Hemorrhage
|
|
|
| Purpura |
|
|
| Endocarditis |
|
|
| Von Willebrand Disease, Type 1 |
|
Von Willebrand Disease Type 1
|
VWD1
|
|
Von Willebrand'S Disease 1
|
Von Willebrand Disease Type I
|
|
Von Willebrand Disease, Type I
|
Vwd, Type 1
|
|
Vwd Type 1
|
Von Willebrand Disease 1
|
|
Von Willebrand Factor Deficiency Type 1
|
Von Willebrand Disease, Type 1, Susceptibility To
|
|
|
| Thrombasthenia |
|
|
| Acquired Thrombocytopenia |
|
Secondary Thrombocytopenia
|
|
|
| Von Willebrand Disease, Type 2 |
|
Von Willebrand Disease Type 2m
|
Von Willebrand Disease Type 2
|
|
Von Willebrand Disease Type 2a
|
Von Willebrand Disease Type 2b
|
|
Von Willebrand Disease Type 2n
|
VWD2
|
|
Von Willebrand'S Disease 2
|
Von Willebrand Disease Type Ii
|
|
Von Willebrand Disease, Type Ii
|
Vwd, Type 2
|
|
Von Willebrand Disease, Types 2a, 2b, 2m, And 2n
|
Vwd Type 2
|
|
Von Willebrand Disease 2
|
Von Willebrand Disease Normandy Variant
|
|
Von Willebrand Disease Type 2 Malmo
|
Von Willebrand Disease Type I New York
|
|
Von Willebrand Factor Deficiency Type 2
|
Vwd2a
|
|
Vwd2b
|
Vwd2m
|
|
Vwd2n
|
Von Willebrand Disease, Type 2a, 2b, 2m, And 2n
|
|
Von Willebrand Disease, Type 2a
|
Von Willebrand Disease, Type 2b
|
|
Von Willebrand Disease, Type 2n
|
|
|
| Acquired Von Willebrand Syndrome |
|
Acquired Von Willebrand Disease
|
Willebrand Disease, Acquired
|
|
Avws
|
|
|
| Hemophilia B |
|
Christmas Disease
|
Factor Ix Deficiency
|
|
F9 Deficiency
|
HEMB
|
|
Plasma Thromboplastin Component Deficiency
|
Congenital Factor Ix Deficiency
|
|
Mild Hemophilia B
|
Severe Hemophilia B
|
|
Congenital Factor Ix Disorder
|
Deficiency, Functional Factor Ix
|
|
Hem B
|
Mild Congenital F9 Deficiency
|
|
Mild Congenital Factor Ix Deficiency
|
Moderate Hemophilia B
|
|
Moderate Congenital F9 Deficiency
|
Moderate Congenital Factor Ix Deficiency
|
|
Severe Congenital F9 Deficiency
|
Severe Congenital Factor Ix Deficiency
|
|
Bleeding Disorder In Hemophilia B Carriers
|
Congenital F9 Deficiency
|
|
Recessive X-Linked Hemophilia B
|
|
|
| Von Willebrand Disease, Type 3 |
|
Von Willebrand Disease Type 3
|
VWD3
|
|
Von Willebrand'S Disease 3
|
Von Willebrand Disease Type Iii
|
|
Von Willebrand Disease, Type Iii
|
Vwd, Type 3
|
|
Vwd Type 3
|
Von Willebrand Disease 3
|
|
Von Willebrand Disease Recessive Form
|
Von Willebrand Factor Deficiency Type 3
|
|
|
| Trimethoprim Allergy |
|
Primsol Allergy
|
Proloprim Allergy
|
|
Tmp Allergy
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Antiphospholipid Syndrome |
|
Antiphospholipid Antibody Syndrome
|
Hughes Syndrome
|
|
Familial Antiphospholipid Syndrome
|
Aps
|
|
Lupus Anticoagulant, Familial
|
Anti-Phospholipid Syndrome
|
|
Apls
|
Classic Apls
|
|
Classic Antiphospholipid Syndrome
|
Acromegaloid Facial Appearance Syndrome
|
|
Anticardiolipin Syndrome
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Erythroleukemia |
|
|
| Myeloproliferative Syndrome, Transient |
|
Transient Abnormal Myelopoiesis
|
Transient Myeloproliferative Syndrome
|
|
Transient Myeloproliferative Disease
|
Mst
|
|
Tam
|
Leukemia, Transient, Of Down Syndrome
|
|
Tmd
|
Leukemia, Transient
|
|
Transient Leukemia
|
Transient Leukemia Of Down Syndrome
|
|
|
| Myh-9 Related Disease |
|
Myh9-Related Disease
|
Myh9-Rd
|
|
Myh9-Related Disorder
|
Myh9-Related Syndrome
|
|
Myh9-Related Syndromic Thrombocytopenia
|
Sebastian Syndrome
|
|
|
| Thrombocytopenia Due To Platelet Alloimmunization |
|
Immune Thrombocytopenia
|
Autoimmune Thrombocytopenia
|
|
Immune Thrombocytopenic Purpura
|
Itp
|
|
Auto-Immune Thrombocytopenia
|
Thrombocytopenia Due To Immune Destruction
|
|
Autoimmune Thrombocytopenic Purpura
|
Idiopathic Thrombocytopenic Purpura
|
|
Werlhof Disease
|
|
|
| Blood Coagulation Disease |
|
Blood Coagulation Disorders
|
Coagulation Protein Disease
|
|
Inherited Blood Coagulation Disease
|
Postpartum Coagulation Defect
|
|
Postpartum Coagulation Defect With Delivery
|
Coagulation Protein Disorders
|
|
Puerperal Coagulopathy
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Qualitative Platelet Defect |
|
Qualitative Platelet Defects
|
Qualitative Platelet Deficiency
|
|
Thrombocytopathy
|
Platelet Defect
|
|
Platelet Disorder
|
Thrombopathy
|
|
Platelet Granule Defect
|
Thrombocytasthenia
|
|
Thromboasthenia
|
Dystrophic Thrombocytopathy
|
|
Haemorrhagic Thrombasthenia
|
Granulopenic Thrombocytopathy
|
|
|
| Meckel Syndrome, Type 6 |
|
Meckel Syndrome 6
|
MKS6
|
|
Meckel-Gruber Syndrome, Type 6
|
|
|
| Polycythemia Vera |
|
PV
|
Polycythemia Rubra Vera
|
|
Prv
|
Osler-Vaquez Disease
|
|
Chronic Erythremia
|
Polycythaemia Rubra Vera
|
|
Primary Polycythemia
|
Vaquez Disease
|
|
Polycythemia Vera, Somatic
|
Osler-Vaquez Syndrome
|
|
Proliferative Polycythaemia
|
Polycythemia Ruba Vera
|
|
Acquired Primary Erythrocytosis
|
Heilmeyer-Schoner Disease
|
|
Vaquez Osler Disease
|
Primary Polycythaemia
|
|
|
| Carotid Artery Thrombosis |
|
|
| Infective Endocarditis |
|
Bacterial Endocarditis
|
Endocarditis, Infective
|
|
Infectious Endocarditis
|
Endocarditis Infective
|
|
|
| Myocardial Infarction |
|
Heart Attack
|
Myocardial Infarction, Susceptibility To
|
|
Myocardial Infarction 1
|
Myocardial Infarction, Protection Against
|
|
Myocardial Infarction, Decreased Susceptibility To
|
Myocardial Infarction, Decreased
|
|
Myocardial Infarct
|
MCI1
|
|
Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Thrombotic Thrombocytopenic Purpura |
|
Purpura, Thrombotic Thrombocytopenic
|
Ttp
|
|
Thrombotic Thrombocytopenic Purpura, Acquired
|
Idiopathic Thrombotic Thrombocytopenic Purpura
|
|
Moschcowitz Disease
|
Moschcowitz'S Syndrome
|
|
Moschowitz Syndrome
|
Chronic Relapsing Thrombotic Thrombocytopenic Purpura
|
|
Familial Thrombotic Thrombocytopenia Purpura
|
Moschkowitz Disease
|
|
Purpura Thrombotic Thrombocytopenic
|
Familial Thrombotic Thrombocytopenic Purpura
|
|
Microangiopathic Hemolytic Anemia
|
Congenital Thrombotic Thrombocytopenic Purpura
|
|
Autoimmune Thrombotic Thrombocytopenic Purpura
|
Ttp - [Thrombotic Thrombocytopenic Purpura]
|
|
Moschcowitz Syndrome
|
|
|
| Childhood Acute Megakaryoblastic Leukemia |
|
Pediatric Non-Down Syndrome Acute Megakaryoblastic Leukemia
|
|
|
| Acrokeratoderma, Hereditary Papulotranslucent |
|
Hereditary Papulotranslucent Acrokeratoderma
|
|
|
| Primary Thrombocytopenia |
|
|
| Amegakaryocytic Thrombocytopenia, Congenital |
|
Congenital Amegakaryocytic Thrombocytopenia
|
CAMT
|
|
Thrombocytopenia, Congenital Amegakaryocytic
|
Congenital Amegakaryocytic Thrombocytopenic Purpura
|
|
Thrombocytopenia Congenital Amegakaryocytic
|
Thrombocytopenia, Amegakaryocytic, Congenital
|
|
|
| Aplastic Anemia |
|
Aplastic Anemia, Susceptibility To
|
Anemia Aplastic
|
|
Idiopathic Aplastic Anemia
|
Secondary Aplastic Anemia
|
|
Idiopathic Bone Marrow Failure
|
Aplastic Anemia Idiopathic
|
|
AA
|
Anemia, Aplastic
|
|
Aplastic Anemia, Idiopathic
|
Erythroid Aplasia
|
|
Aa - [Aplastic Anaemia]
|
Haematopoietic Aplasia
|
|
Aleukia Haemorrhagica
|
Anaemia Due To Decreased Red Cell Production
|
|
Aplasia Bone Marrow
|
Aplastic Bone Marrow
|
|
Hypoplastic Anaemia Nos
|
Myeloid Bone Marrow Aplasia
|
|
Pancytopenia
|
Panhaematopenia
|
|
Hypoproliferative Anaemia
|
Medullary Hypoplasia
|
|
Red Blood Cells Hypoplastic Anaemia
|
Panmyelophthisis
|
|
Panhemocytopenia
|
Refractive Hypoproliferative Anaemia
|
|
Toxic Anaemia
|
Toxic Aplastic Anaemia
|
|
Aplastic Anaemia Due To Toxic Cause
|
Idiopathic Aplastic Anaemia Nos
|
|
|
| Acute Megakaryocytic Leukemia |
|
Acute Megakaryoblastic Leukemia
|
Acute Megakaryoblastic Leukaemia
|
|
Megakaryocytic Myelosis
|
Thrombocytic Leukaemia
|
|
Amkl
|
Aml M7
|
|
Acute Myeloblastic Leukemia Type 7
|
Acute Myeloid Leukemia M7
|
|
Megakaryoblastic Leukemia Acute
|
Leukemia, Megakaryoblastic, Acute
|
|
Acute Myeloid Leukaemia, M7
|
Acute Megakaryocytic Leukaemia
|
|
Acute Megakaryoblastic Leukaemia, Fab M7
|
Fab M7
|
|
Malignant Megakaryocytosis
|
M7 - Acute Megakaryoblastic Leukaemia
|
|
Megakaryoblastic Leukaemia
|
Megakaryocytic Leukaemia
|
|
Acute Megakaryoblastic Leukaemia, Nos
|
Acute Megakaryoblastic Leukaemia Without Mention Of Remission
|
|
|
| Jacobsen Syndrome |
|
Chromosome 11q Deletion Syndrome
|
Partial 11q Monosomy Syndrome
|
|
Jacobsen Distal 11q Deletion Syndrome
|
JBS
|
|
11q Partial Monosomy Syndrome
|
Chromosome 11q Deletion
|
|
11q Deletion
|
11q Monosomy
|
|
Deletion 11q
|
Monosomy 11q
|
|
Partial Monosomy 11q
|
11q Deletion Disorder
|
|
11q Deletion Syndrome
|
11q Terminal Deletion Disorder
|
|
11q- Deletion Syndrome
|
11q23 Deletion Disorder
|
|
Jacobsen Thrombocytopenia
|
11q Terminal Deletion Syndrome
|
|
Del(11)(Q23.3)
|
Del(11)(Qter)
|
|
Distal Deletion 11q
|
Distal Monosomy 11q
|
|
Monosomy 11qter
|
Telomeric Deletion 11q
|
|
Paris-Trousseau Thrombocytopenia
|
|
|
| Diabetes Mellitus |
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Stroke, Ischemic |
|
Cerebral Infarction
|
Stroke
|
|
Ischemic Stroke
|
Cerebrovascular Accident
|
|
Cerebral Infarction, Susceptibility To
|
Stroke, Ischemic, Susceptibility To
|
|
Cerebral Infarct
|
Ischemic Stroke, Susceptibility To
|
|
Stroke, Susceptibility To
|
Cva - Cerebral Infarction
|
|
ISCHSTR
|
Ischemic Cerebrovascular Accident
|
|
|
| Essential Thrombocythemia |
|
Essential Thrombocytosis
|
Familial Thrombocytosis
|
|
Hemorrhagic Thrombocythemia
|
Hereditary Thrombocythemia
|
|
Primary Thrombocytosis
|
Idiopathic Thrombocythemia
|
|
Primary Thrombocythemia
|
Thrombocythemia, Essential
|
|
Essential Thrombocythaemia
|
Et
|
|
Familial Thrombocythemia
|
Thrombocythemia Essential
|
|
|
| Myelodysplastic Syndrome |
|
Myelodysplastic Syndromes
|
Myelodysplasia
|
|
MDS
|
Myelodysplastic Syndrome Included
|
|
Myelodysplastic Syndrome, Susceptibility To, Included
|
Myelodysplastic Syndrome, Somatic
|
|
Myelodysplastic Syndrome, Susceptibility To
|
|
|
