| 疾病名称 |
别名 |
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| Thrombosis |
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Thrombosis Of Blood Vessel
|
|
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| Stroke, Ischemic |
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Cerebral Infarction
|
Stroke
|
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Ischemic Stroke
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Cerebrovascular Accident
|
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Cerebral Infarction, Susceptibility To
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Stroke, Ischemic, Susceptibility To
|
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Cerebral Infarct
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Ischemic Stroke, Susceptibility To
|
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Stroke, Susceptibility To
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Cva - Cerebral Infarction
|
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ISCHSTR
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Ischemic Cerebrovascular Accident
|
|
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| Prostate Cancer |
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Prostate Carcinoma
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Prostate Cancer, Familial
|
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Prostate Neoplasm
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Prostate Cancer, Somatic
|
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Prostate Cancer, Susceptibility To
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Prostatic Cancer
|
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Prostatic Neoplasms
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Hereditary Prostate Cancer
|
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Prostatic Neoplasm
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Cancer Of Prostate
|
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Carcinoma Of Prostate
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Familial Prostate Cancer
|
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Familial Prostate Carcinoma
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Malignant Tumor Of Prostate
|
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Malignant Neoplasm Of Prostate
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Prostate Cancer, Familial, Susceptibility To
|
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Malignant Tumor Of The Prostate
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Ngp - New Growth Of Prostate
|
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Tumor Of The Prostate
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Prostate Cancer, Hereditary
|
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Cancer Of The Prostate
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Malignant Neoplasm Of The Prostate
|
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Prostatic Carcinoma
|
PC
|
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Prca
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Cancer, Prostate
|
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Malignant Prostatic Tumour
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Malignant Tumour Of Prostate
|
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Primary Prostate Cancer
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Primary Malignant Neoplasm Of Prostate
|
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Prostate Gland Cancer
|
|
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| Peroxisome Biogenesis Disorder 1b |
|
Peroxisome Biogenesis Disorder
|
Infantile Refsum Disease
|
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Infantile Phytanic Acid Storage Disease
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PBD1B
|
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Refsum Disease, Infantile
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Adrenoleukodystrophy, Autosomal Neonatal
|
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Ird
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Mild Pbd-Zsd
|
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Mild Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder
|
Pbd-Zsd
|
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Peroxisome Biogenesis Disorder Spectrum
|
Peroxisome Biogenesis Disorder-Zellweger Spectrum Disorder
|
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Autosomal Neonatal Adrenoleukodystrophy
|
Refsum Disease Infantile
|
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Peroxisome Biogenesis Disorders
|
Peroxisome Biogenesis Disorder, Type 1b
|
|
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| Hypertension, Essential |
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Essential Hypertension
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Hypertension
|
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High Blood Pressure
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Hypertension, Essential, Susceptibility To
|
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Hypertensive Disease
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Primary Hypertension
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EHT
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Hypertension, Salt-Sensitive Essential, Susceptibility To
|
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Hyperpiesia
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Idiopathic Hypertension
|
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Hypertensive Disorder
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Hypertension, Essential, Susceptibility To, 3
|
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Hypertension, Essential 3
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Hypertension, Essential, Salt-Sensitive
|
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Hypertension, Essential, Susceptibility To, 6
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Hypertension, Essential 6
|
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Hypertension, Salt-Sensitive Essential
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Hypertension, Susceptibility To
|
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Hypertension, Essential, Susceptibility To, 4
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Hypertension, Essential 4
|
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Hypertension, Essential, Susceptibility To, 2
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Hypertension, Essential 2
|
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Hypertension, Essential, Susceptibility To, 1
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Hypertension, Essential 1
|
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Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
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Htn
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Vascular Hypertensive Disorder
|
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Systemic Primary Arterial Hypertension
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Hbp - [High Blood Pressure]
|
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Systemic Arterial Hypertensive Disorder
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Elevated Blood Pressure
|
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Arterial Hypertension Nos
|
Hypertension Nos
|
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Benign Hypertension
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Systemic Arterial Hypertension
|
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Systemic Hypertension
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Artery Htn
|
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Benign Htn
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Vascular Htn
|
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Vascular Hypertension
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Cholesterol Hypertension
|
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Cholesterol Htn
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Idiopathic Htn
|
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Malignant Hypertension
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Malignant Htn
|
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Raised Blood Pressure
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Cardiovascular Hypertension
|
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Primary Htn - [Hypertension]
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High Arterial Tension
|
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High Blood Pressure Disorder
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Ht - [Hypertension]
|
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Htn - [Hypertension]
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Hypertensive Vascular Disease
|
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Hypertensive Vascular Degeneration
|
|
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| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
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Malignant Tumour Of Ovary
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Epithelial Ovarian Cancer
|
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Neoplasm Of Ovary
|
Ovarian Neoplasms
|
|
Ovarian Cancers
|
Malignant Neoplasm Of Ovary
|
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Primary Malignant Neoplasm Of Ovary
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Ovarian Cancer, Somatic
|
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Malignant Ovarian Tumor
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Ovary Neoplasm
|
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Primary Ovarian Cancer
|
Tumor Of The Ovary
|
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Cancer Of The Ovary
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Malignant Neoplasm Of The Ovary
|
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Malignant Tumor Of The Ovary
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Ovarian Malignant Tumor
|
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OC
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Ovarian Carcinomas
|
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Cancer, Ovarian
|
Cancer Of Ovary
|
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Ovary Cancer
|
Ca Ovary
|
|
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| Chromosome 5q Deletion Syndrome |
|
5q- Syndrome
|
Mar
|
|
Myelodysplastic Syndrome Associated With Isolated Del Chromosome Abnormality
|
Macrocytic Anemia, Refractory, Due To 5q Deletion, Somatic
|
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5q Deletion Syndrome
|
5q Minus Syndrome
|
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Refractory Macrocytic Anemia Due To 5q Deletion
|
Myelodysplastic Syndrome With Isolated Del
|
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Macrocytic Anemia, Refractory, Due To 5q Deletion
|
5q- Syndrome, Refractory Macrocytic Anemia Due To 5q Deletion
|
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5q Syndrome
|
Chromosome 5q Deletion
|
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Myelodysplastic Syndrome With 5q Deletion
|
Myelodysplastic Syndrome With 5q Deletion Syndrome
|
|
Anemia, Macrocytic, Refractory, Due To 5q Deletion, Somatic
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5q-Syndrome
|
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Chromosome 5, Trisomy 5q
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Loss Of Chromosome 5q
|
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5 Q- Syndrome
|
|
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| Blood Platelet Disease |
|
Platelet Disorder
|
Blood Platelet Disorders
|
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Thrombocytopathy
|
Platelet Dysfunction
|
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Platelet Disorders
|
Qualitative Platelet Deficiency
|
|
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| Peripheral Artery Disease |
|
Peripheral Arterial Disease
|
Peripheral Arterial Diseases
|
|
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| Bernard-Soulier Syndrome |
|
Giant Platelet Syndrome
|
BSS
|
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Von Willebrand Factor Receptor Deficiency
|
Bdplt1
|
|
Platelet Glycoprotein Ib Deficiency
|
Bernard-Soulier Syndrome, Type A1
|
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Bernard-Soulier Syndrome, Type B
|
Bernard Soulier Syndrome
|
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Deficiency Of Platelet Glycoprotein 1b
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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
|
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Bernard-Soulier Syndrome, Type C
|
Bernard - Soulier Thrombopathy
|
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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
|
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Macrothrombocytopenia, Familial, Bernard-Soulier Type
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Spinal Cord Vascular Diseases
|
|
Vascular Tissue Disease
|
Vascular Anomaly
|
|
|
| Glanzmann Thrombasthenia 1 |
|
Glanzmann Thrombasthenia
|
Thrombasthenia Of Glanzmann And Naegeli
|
|
Bdplt2
|
Platelet Glycoprotein Iib-Iiia Deficiency
|
|
Glanzmann'S Thrombasthenia
|
Deficiency Of Platelet Fibrinogen Receptor
|
|
GT1
|
Gt
|
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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
|
|
|
| Pulmonary Fibrosis |
|
|
| 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
|
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Premature Myocardial Infarction
|
Myocardial Infarction, Susceptibility To, Type 1
|
|
|
| Bleeding Disorder, Platelet-Type, 20 |
|
Platelet-Type Bleeding Disorder 20
|
BDPLT20
|
|
Autosomal Dominant Thrombocytopenia With Platelet Secretion Defect
|
|
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| Thrombocytopenia |
|
Low Platelet Count
|
Low Platelets
|
|
Decreased Platelets
|
Platelet Dysfunction Nos
|
|
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| Carotid Artery Disease |
|
Carotid Artery Diseases
|
Disorder Of Carotid Artery
|
|
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| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
BMIQ11
|
Obesity Bmiq11
|
|
Obesity, Early-Onset
|
Obesity , Susceptibility To
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Disease, Susceptibility To
|
|
Coronary Artery Anomaly
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
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Coronary Disease
|
Coronary Heart Disease
|
|
Coronary Artery Disorder
|
LPAQTL
|
|
Lpa Deficiency, Congenital
|
Coronary Artery Abnormality
|
|
Coronary Artery Anomaly, Congenital
|
Chd
|
|
Coronary Syndrome
|
Congenital Malformations Of Coronary Vessels
|
|
Malformation Of Coronary Vessels
|
Congenital Coronary Artery Anomaly
|
|
Congenital Coronary Artery Deformity
|
Congenital Coronary Artery Disorder
|
|
Abnormal Coronary Artery
|
Congenital Coronary Artery Malposition
|
|
Congenital Coronary Disease
|
Congenital Anomaly Of Coronary Arteries
|
|
|
| Alpha-2-Plasmin Inhibitor Deficiency |
|
Plasmin Inhibitor Deficiency
|
Antiplasmin Deficiency
|
|
Antiplasmin Defiency
|
Anti-Plasmin Deficiency, Congenital
|
|
Antiplasmin Deficiency, Congenital
|
Congenital Alpha2-Antiplasmin Deficiency
|
|
APLID
|
Congenital Alpha2 Antiplasmin Deficiency
|
|
|
| Carotid Artery Thrombosis |
|
|
