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| Boli A-Z | | 3-Methylglutaconic Aciduria
3-Methylglutaconic Aciduria, Type I
3-Methylglutaconic Aciduria, Type Iii
3-Methylglutaconic Aciduria, Type Iv
3-Methylglutaconic Aciduria, Type Ix
3-Methylglutaconic Aciduria, Type V
3-Methylglutaconic Aciduria, Type Viii
Abnormal Number of Coronary Ostia
Absence of Innominate Vein
Absence of the Pulmonary Artery
Accessory Mitral Valve Tissue
Accessory Tricuspid Valve Tissue
Achalasia
Acquired Cutis Laxa
Acquired Pseudoxanthoma Elasticum
Acute Anterolateral Myocardial Infarction
Acute Conjunctivitis
Acute Cor Pulmonale
Acute Inferolateral Myocardial Infarction
Acute Inferoposterior Infarction
Acute Myocardial Infarction
Acute Myocarditis
Acute Pulmonary Heart Disease
Acute Respiratory Distress Syndrome
Acute Vascular Insufficiency of Intestine
Adenosine Deaminase 2 Deficiency
Adrenocortical Carcinoma, Hereditary
Adult Acute Respiratory Distress Syndrome
Adult Respiratory Distress Syndrome
Agenesis of the Superior Vena Cava
Alagille Syndrome 1
Alagille Syndrome 2
Alcoholic Cardiomyopathy
Al-Gazali Syndrome
Allergic Cutaneous Vasculitis
Alveolar Capillary Dysplasia
Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins
Amyloidosis, Hereditary, Transthyretin-Related
Anca-Associated Vasculitis
Andersen Cardiodysrhythmic Periodic Paralysis
Aneurysm, Intracranial Berry, 1
Aneurysm, Intracranial Berry, 10
Aneurysm, Intracranial Berry, 11
Aneurysm, Intracranial Berry, 2
Aneurysm, Intracranial Berry, 3
Aneurysm, Intracranial Berry, 4
Aneurysm, Intracranial Berry, 5
Aneurysm, Intracranial Berry, 6
Aneurysm, Intracranial Berry, 7
Aneurysm, Intracranial Berry, 8
Aneurysm, Intracranial Berry, 9
Aneurysm of Interventricular Septum
Aneurysm of Sinus of Valsalva
Aneurysm or Dilatation of Ascending Aorta
Angina Pectoris
Angiodysplasia
Angiodysplasia of Intestine
Angioma, Hereditary Neurocutaneous
Angioma Serpiginosum
Angioma Serpiginosum, Autosomal Dominant
Angioma, Tufted
Angiomyoma
Angioosteohypertrophic Syndrome
Angioosteohypotrophic Syndrome
Angiosarcoma
Anomalous Left Coronary Artery from the Pulmonary Artery
Anomaly of the Mitral Subvalvular Apparatus
Anomaly of the Tricuspid Valve Chordae
Anophthalmia Megalocornea Cardiopathy Skeletal Anomalies
Anterior Cerebral Artery Infarction
Anterior Compartment Syndrome
Anterior Spinal Artery Syndrome
Anterolateral Myocardial Infarction
Anteroseptal Myocardial Infarction
Aorta Atresia
Aortic Aneurysm
Aortic Aneurysm, Familial Abdominal, 1
Aortic Aneurysm, Familial Abdominal, 2
Aortic Aneurysm, Familial Abdominal, 3
Aortic Aneurysm, Familial Abdominal, 4
Aortic Aneurysm, Familial Thoracic 1
Aortic Aneurysm, Familial Thoracic 10
Aortic Aneurysm, Familial Thoracic 11
Aortic Aneurysm, Familial Thoracic 2
Aortic Aneurysm, Familial Thoracic 4
Aortic Aneurysm, Familial Thoracic 6
Aortic Aneurysm, Familial Thoracic 7
Aortic Aneurysm, Familial Thoracic 8
Aortic Aneurysm, Familial Thoracic 9
Aortic Arch Interruption
Aortic Atherosclerosis
Aortic Disease
Aortic Valve Atresia
Aortic Valve Disease 1
Aortic Valve Disease 2
Aortic Valve Dysplasia
Aortic Valve Insufficiency
Aortic Valve Prolapse
Aortitis
Aorto-Left Ventricular Tunnel
Aortopulmonary Coronary Arterial Course
Aortopulmonary Window
Aorto-Right Ventricular Tunnel
Aorto-Ventricular Tunnel
Apical Myocardial Infarction
Aplasia Cutis Congenita with Intestinal Lymphangiectasia
Apparent Mineralocorticoid Excess
Arrhythmogenic Right Ventricular Cardiomyopathy
Arrhythmogenic Right Ventricular Dysplasia, Familial, 1
Arrhythmogenic Right Ventricular Dysplasia, Familial, 10
Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
Arrhythmogenic Right Ventricular Dysplasia, Familial, 12
Arrhythmogenic Right Ventricular Dysplasia, Familial, 13
Arrhythmogenic Right Ventricular Dysplasia, Familial, 2
Arrhythmogenic Right Ventricular Dysplasia, Familial, 3
Arrhythmogenic Right Ventricular Dysplasia, Familial, 4
Arrhythmogenic Right Ventricular Dysplasia, Familial, 5
Arrhythmogenic Right Ventricular Dysplasia, Familial, 6
Arrhythmogenic Right Ventricular Dysplasia, Familial, 8
Arrhythmogenic Right Ventricular Dysplasia, Familial, 9
Arterial Calcification, Generalized, of Infancy, 1
Arterial Calcification, Generalized, of Infancy, 2
Arterial Calcification of Infancy
Arterial Dissection with Lentiginosis
Arterial Tortuosity Syndrome
Arteries, Anomalies of
Arteriolosclerosis
Arteriosclerosis
Arteriosclerosis Obliterans
Arteriosclerosis, Severe Juvenile
Arteriovenous Fistula
Arteriovenous Malformations of the Brain
Ascites, Chylous
Aspirin Resistance
Ataxia, Deafness, and Cardiomyopathy
Athabaskan Brainstem Dysgenesis Syndrome
Atheroembolism of Kidney
Atherosclerosis Susceptibility
Atrial Fibrillation
Atrial Fibrillation, Familial, 1
Atrial Fibrillation, Familial, 10
Atrial Fibrillation, Familial, 11
Atrial Fibrillation, Familial, 12
Atrial Fibrillation, Familial, 13
Atrial Fibrillation, Familial, 14
Atrial Fibrillation, Familial, 15
Atrial Fibrillation, Familial, 18
Atrial Fibrillation, Familial, 2
Atrial Fibrillation, Familial, 3
Atrial Fibrillation, Familial, 4
Atrial Fibrillation, Familial, 5
Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 7
Atrial Fibrillation, Familial, 8
Atrial Fibrillation, Familial, 9
Atrial Heart Septal Defect
Atrial Heart Septal Defect 7
Atrial Septal Aneurysm
Atrial Septal Defect 1
Atrial Septal Defect 2
Atrial Septal Defect 3
Atrial Septal Defect 4
Atrial Septal Defect 5
Atrial Septal Defect 6
Atrial Septal Defect 7 with or Without Atrioventricular Conduction Defects
Atrial Septal Defect 8
Atrial Septal Defect 9
Atrial Septal Defect Coronary Sinus
Atrial Septal Defect Ostium Primum
Atrial Septal Defect Sinus Venosus
Atrial Standstill
Atrial Standstill 1
Atrial Standstill 2
Atrioventricular Block
Atrioventricular Septal Defect
Atrioventricular Septal Defect 2
Atrioventricular Septal Defect 3
Atrioventricular Septal Defect 4
Atrioventricular Septal Defect 5
Atrioventricular Septal Defect with Blepharophimosis and Anal and Radial Defects
Atypical Coarctation of Aorta
Autoimmune Disease of Cardiovascular System
Autoimmune Myocarditis
Autosomal Dominant Coarctation of Aorta
Autosomal Dominant Nonsyndromic Deafness
Autosomal Recessive Nonsyndromic Deafness
Autosomal Recessive Nonsyndromic Deafness 3
Autosomal Recessive Nonsyndromic Deafness 36
Autosomal Recessive Nonsyndromic Deafness 86
Azygos Continuation of the Inferior Vena Cava
Bacterial Conjunctivitis
Bannayan-Riley-Ruvalcaba Syndrome
Barth Syndrome
Basal Ganglia Calcification, Idiopathic, 1
Basal Ganglia Calcification, Idiopathic, 2
Basal Ganglia Calcification, Idiopathic, 4
Basal Ganglia Calcification, Idiopathic, 5
Basal Ganglia Calcification, Idiopathic, 6
Basal Ganglia Cerebrovascular Disease
Basilar Artery Insufficiency
Basilar Artery Occlusion
Behcet Syndrome
Benign Angiitis of the Central Nervous System
Benign Essential Hypertension
Benign Hypertensive Renal Disease
Benign Renovascular Hypertension
Benign Secondary Hypertension
Blue Rubber Bleb Nevus
Blue Toe Syndrome
Brain Malformation-Congenital Heart Disease-Postaxial Polydactyly Syndrome
Brain Small Vessel Disease with or Without Ocular Anomalies
Brain Stem Angioblastoma
Brain Stem Infarction
Branch Retinal Artery Occlusion
Breast Angiomatosis
Broken Heart Syndrome
Brugada Syndrome
Brugada Syndrome 1
Brugada Syndrome 2
Brugada Syndrome 3
Brugada Syndrome 4
Brugada Syndrome 5
Brugada Syndrome 6
Brugada Syndrome 7
Brugada Syndrome 8
Brugada Syndrome 9
Budd-Chiari Syndrome
Buerger Disease
Calcification of Joints and Arteries
Calciphylaxis
Calciphylaxis Cutis
Campomelia, Cumming Type
Campomelic Dysplasia
Cantú Syndrome and Related Disorders
Cantu Syndrome
Capillary Disease
Capillary Hemangioma
Capillary Leak Syndrome
Capillary Lymphangioma
Capillary Malformation-Arteriovenous Malformation
Capillary Malformation of the Lower Lip, Lymphatic Malformation of Face and Neck, Asymmetry of Face and Limbs, and Partial/generalized Overgrowth
Capillary Malformations, Congenital
Cardiac Anomalies-Heterotaxy Syndrome
Cardiac Arrest
Cardiac Conduction Disease with or Without Dilated Cardiomyopathy
Cardiac Diverticulum
Cardiac Tamponade
Cardiac Tuberculosis
Cardiac Valvular Dysplasia, X-Linked
Cardioauditory Syndrome of Sanchez Cascos
Cardiocranial Syndrome
Cardioencephalomyopathy
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 1
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 2
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 3
Cardioencephalomyopathy, Fatal Infantile, Due to Cytochrome C Oxidase Deficiency 4
Cardiofacial Syndrome Short Limbs
Cardiofaciocutaneous Syndrome 1
Cardiofaciocutaneous Syndrome 2
Cardiofaciocutaneous Syndrome 3
Cardiofaciocutaneous Syndrome 4
Cardiogenic Shock
Cardiomelic Syndrome Stratton Koehler Type
Cardiomyopathy and Deafness Due to Trna Lysine Gene Mutation
Cardiomyopathy Associated with Myopathy and Sudden Death
Cardiomyopathy Cataract Hip Spine Disease
Cardiomyopathy Diabetes Deafness
Cardiomyopathy, Dilated, 1a
Cardiomyopathy, Dilated, 1aa, with or Without Left Ventricular Noncompaction
Cardiomyopathy, Dilated, 1b
Cardiomyopathy, Dilated, 1bb
Cardiomyopathy, Dilated, 1cc
Cardiomyopathy, Dilated, 1c, with or Without Left Ventricular Noncompaction
Cardiomyopathy, Dilated, 1d
Cardiomyopathy, Dilated, 1dd
Cardiomyopathy, Dilated, 1e
Cardiomyopathy, Dilated, 1ee
Cardiomyopathy, Dilated, 1ff
Cardiomyopathy, Dilated, 1g
Cardiomyopathy, Dilated, 1gg
Cardiomyopathy, Dilated, 1h
Cardiomyopathy, Dilated, 1hh
Cardiomyopathy, Dilated, 1i
Cardiomyopathy, Dilated, 1ii
Cardiomyopathy, Dilated, 1j
Cardiomyopathy, Dilated, 1jj
Cardiomyopathy, Dilated, 1k
Cardiomyopathy, Dilated, 1kk
Cardiomyopathy, Dilated, 1l
Cardiomyopathy, Dilated, 1m
Cardiomyopathy, Dilated, 1nn
Cardiomyopathy, Dilated, 1o
Cardiomyopathy, Dilated, 1p
Cardiomyopathy, Dilated, 1q
Cardiomyopathy, Dilated, 1r
Cardiomyopathy, Dilated, 1u
Cardiomyopathy, Dilated, 1v
Cardiomyopathy, Dilated, 1w
Cardiomyopathy, Dilated, 1x
Cardiomyopathy, Dilated, 1z
Cardiomyopathy, Dilated, 2a
Cardiomyopathy, Dilated, 2b
Cardiomyopathy, Dilated, 3b
Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism
Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma
Cardiomyopathy, Dilated, with Woolly Hair, Keratoderma, and Tooth Agenesis
Cardiomyopathy Due to Anthracyclines
Cardiomyopathy, Familial Hypertrophic, 1
Cardiomyopathy, Familial Hypertrophic, 10
Cardiomyopathy, Familial Hypertrophic, 11
Cardiomyopathy, Familial Hypertrophic, 12
Cardiomyopathy, Familial Hypertrophic, 13
Cardiomyopathy, Familial Hypertrophic, 14
Cardiomyopathy, Familial Hypertrophic, 15
Cardiomyopathy, Familial Hypertrophic, 16
Cardiomyopathy, Familial Hypertrophic, 17
Cardiomyopathy, Familial Hypertrophic, 18
Cardiomyopathy, Familial Hypertrophic, 19
Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Familial Hypertrophic, 21
Cardiomyopathy, Familial Hypertrophic, 25
Cardiomyopathy, Familial Hypertrophic, 26
Cardiomyopathy, Familial Hypertrophic, 3
Cardiomyopathy, Familial Hypertrophic, 4
Cardiomyopathy, Familial Hypertrophic, 6
Cardiomyopathy, Familial Hypertrophic, 7
Cardiomyopathy, Familial Hypertrophic, 8
Cardiomyopathy, Familial Hypertrophic, 9
Cardiomyopathy, Familial Restrictive, 1
Cardiomyopathy, Familial Restrictive, 2
Cardiomyopathy, Familial Restrictive, 3
Cardiomyopathy, Fatal Fetal, Due to Myocardial Calcification
Cardiomyopathy Hypogonadism Metabolic Anomalies
Cardiomyopathy, Infantile Histiocytoid
Cardiomyopathy, Infantile Hypertrophic
Cardiomyopathy-Renal Anomalies Syndrome
Cardiomyopathy Spherocytosis
Cardioneuromyopathy with Hyaline Masses and Nemaline Rods
Cardioskeletal Syndrome, Kuwaiti Type
Cardiospondylocarpofacial Syndrome
Cardiovascular Organ Benign Neoplasm
Cardiovascular Syphilis
Carotid Artery Disease
Carotid Artery Dissection
Carotid Artery Occlusion
Carotid Artery Thrombosis
Carotid Stenosis
Catecholaminergic Polymorphic Ventricular Tachycardia
Catecholaminergic Polymorphic Ventricular Tachycardia 5
Cavernous Sinus Thrombosis
Cayler Cardiofacial Syndrome
Central Nervous System Vasculitis
Central Retinal Artery Occlusion
Central Retinal Vein Occlusion
Cerebellar Angioblastoma
Cerebral Amyloid Angiopathy, Cst3-Related
Cerebral Arterial Disease
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1
Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2
Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy
Cerebral Arteritis
Cerebral Artery Occlusion
Cerebral Atherosclerosis
Cerebrofacial Arteriovenous Metameric Syndrome Type 1
Cerebrofacial Arteriovenous Metameric Syndrome Type 3
Cerebrovascular Disease
Cervical Aortic Arch
Char Syndrome
Choanal Atresia and Lymphedema
Cholestasis-Lymphedema Syndrome
Cholesterol Embolism
Chops Syndrome
Chromosome 17q11.2 Deletion Syndrome, 1.4-Mb
Chronic Conjunctivitis
Chronic Intestinal Vascular Insufficiency
Chronic Orthostatic Intolerance
Chronic Pulmonary Heart Disease
Chronic Rheumatic Pericarditis
Chronic Venous Insufficiency
Churg-Strauss Syndrome
Cirrhotic Cardiomyopathy
Cleft Lip and Palate Malrotation Cardiopathy
Cleft Lip/palate with Characteristic Facies, Intestinal Malrotation, and Lethal Congenital Heart Disease
Cleft Mitral Valve
Coarctation of Aorta
Cobb Syndrome
Coenzyme Q10 Deficiency, Primary, 5
Coenzyme Q10 Deficiency, Primary, 7
Cogan Syndrome
Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome
Combined Oxidative Phosphorylation Deficiency 10
Combined Oxidative Phosphorylation Deficiency 16
Combined Oxidative Phosphorylation Deficiency 28
Combined Oxidative Phosphorylation Deficiency 3
Combined Oxidative Phosphorylation Deficiency 8
Compartment Syndrome
Complete Atrioventricular Canal
Complete Atrioventricular Canal-Left Heart Obstruction Syndrome
Complete Atrioventricular Canal-Tetralogy of Fallot Syndrome
Complete Atrioventricular Canal-Ventricle Hypoplasia Syndrome
Composite Hemangioendothelioma
Congenital Anomaly of Hepatic Vein
Congenital Aortic Valve Insufficiency
Congenital Aortopulmonary Window
Congenital Cardiovascular Shunt
Congenital Cataract-Hypertrophic Cardiomyopathy-Mitochondrial Myopathy Syndrome
Congenital Complete Agenesis of Pericardium
Congenital Coronary Artery Aneurysm
Congenital Disorder of Glycosylation, Type Ia
Congenital Disorder of Glycosylation, Type Ib
Congenital Disorder of Glycosylation, Type Ic
Congenital Disorder of Glycosylation, Type Id
Congenital Disorder of Glycosylation, Type Ie
Congenital Disorder of Glycosylation, Type if
Congenital Disorder of Glycosylation, Type Ig
Congenital Disorder of Glycosylation, Type Ih
Congenital Disorder of Glycosylation, Type Ii
Congenital Disorder of Glycosylation, Type Iia
Congenital Disorder of Glycosylation, Type Iib
Congenital Disorder of Glycosylation, Type Iic
Congenital Disorder of Glycosylation, Type Iid
Congenital Disorder of Glycosylation, Type Iif
Congenital Disorder of Glycosylation, Type Iig
Congenital Disorder of Glycosylation, Type Iih
Congenital Disorder of Glycosylation, Type Iii
Congenital Disorder of Glycosylation, Type I/iix
Congenital Disorder of Glycosylation, Type Iij
Congenital Disorder of Glycosylation, Type Iik
Congenital Disorder of Glycosylation, Type Iil
Congenital Disorder of Glycosylation, Type Iim
Congenital Disorder of Glycosylation, Type Iin
Congenital Disorder of Glycosylation, Type Iio
Congenital Disorder of Glycosylation, Type Iip
Congenital Disorder of Glycosylation, Type Iiq
Congenital Disorder of Glycosylation, Type Ij
Congenital Disorder of Glycosylation, Type Ik
Congenital Disorder of Glycosylation, Type Il
Congenital Disorder of Glycosylation, Type Im
Congenital Disorder of Glycosylation, Type in
Congenital Disorder of Glycosylation, Type Io
Congenital Disorder of Glycosylation, Type Ip
Congenital Disorder of Glycosylation, Type Iq
Congenital Disorder of Glycosylation, Type Ir
Congenital Disorder of Glycosylation, Type It
Congenital Disorder of Glycosylation, Type Iu
Congenital Disorder of Glycosylation, Type Iw
Congenital Disorder of Glycosylation, Type Ix
Congenital Disorder of Glycosylation, Type Iy
Congenital Gerbode Defect
Congenital Heart Defects, Multiple Types, 2
Congenital Heart Defects, Multiple Types, 3
Congenital Heart Defects, Multiple Types, 4
Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi
Congenitally Corrected Transposition of the Great Arteries
Congenitally Uncorrected Transposition of the Great Arteries with Cardiac Malformation
Congenitally Uncorrected Transposition of the Great Arteries with Coarctation
Congenital Mitral Stenosis
Congenital Muscular Dystrophy Due to Dystroglycanopathy
Congenital Muscular Dystrophy Type 1a
Congenital Partial Agenesis of Pericardium
Congenital Partial Pulmonary Venous Return Anomaly
Congenital Patent Ductus Arteriosus Aneurysm
Congenital Portosystemic Shunt
Congenital Pulmonary Veins Atresia or Stenosis
Congenital Renal Artery Stenosis
Congenital Stenosis of the Inferior Vena Cava
Congenital Supravalvular Mitral Ring
Congenital Systemic Arteriovenous Fistula
Congenital Tricuspid Stenosis
Congenital Unguarded Mitral Orifice
Congenital Vascular Cavernous Malformations
Congestive Heart Failure
Conjunctival Vascular Disease
Conjunctivitis
Conotruncal Heart Malformations
Constrictive Pericarditis
Coronary Aneurysm
Coronary Arterial Fistulas
Coronary Artery Aneurysm
Coronary Artery Anomaly
Coronary Artery Disease, Autosomal Dominant, 1
Coronary Artery Disease, Autosomal Dominant 2
Coronary Artery Dissection, Spontaneous
Coronary Artery Intramyocardial Course
Coronary Artery Vasospasm
Coronary Restenosis
Coronary Sinus Atresia
Coronary Sinus Stenosis
Coronary Stenosis
Coronary Thrombosis
Cor Triatriatum
Cor Triatriatum Dexter
Cor Triatriatum Sinister
Costello Syndrome
Craniostenosis, Sagittal, with Congenital Heart Disease, Mental Deficiency, and Mandibular Ankylosis
Criss-Cross Heart
Cryoglobulinemia, Familial Mixed
Cutaneous Polyarteritis Nodosa
Cutaneus Colagenous Vasculopathy
Cutis Laxa
Cutis Laxa, Autosomal Dominant 1
Cutis Laxa, Autosomal Dominant 2
Cutis Laxa, Autosomal Dominant 3
Cutis Laxa, Autosomal Recessive Type 1
Cutis Laxa, Autosomal Recessive, Type Ia
Cutis Laxa, Autosomal Recessive, Type Ib
Cutis Laxa, Autosomal Recessive, Type Ic
Cutis Laxa, Autosomal Recessive, Type Iia
Cutis Laxa, Autosomal Recessive, Type Iib
Cutis Laxa, Autosomal Recessive, Type Iic
Cutis Laxa, Autosomal Recessive, Type Iid
Cutis Laxa, Autosomal Recessive, Type Iiia
Cutis Laxa, Autosomal Recessive, Type Iiib
Cutis Marmorata Telangiectatica Congenita
Cystic Angiomatosis of Bone, Diffuse
Cystic Lymphangioma
Danon Disease
Deafness, Autosomal Dominant 1
Deafness, Autosomal Dominant 10
Deafness, Autosomal Dominant 11
Deafness, Autosomal Dominant 12
Deafness, Autosomal Dominant 13
Deafness, Autosomal Dominant 15
Deafness, Autosomal Dominant 16
Deafness, Autosomal Dominant 17
Deafness, Autosomal Dominant 18
Deafness, Autosomal Dominant 20
Deafness, Autosomal Dominant 21
Deafness, Autosomal Dominant 22
Deafness, Autosomal Dominant 23
Deafness, Autosomal Dominant 24
Deafness, Autosomal Dominant 25
Deafness, Autosomal Dominant 27
Deafness, Autosomal Dominant 28
Deafness, Autosomal Dominant 2a
Deafness, Autosomal Dominant 2b
Deafness, Autosomal Dominant 30
Deafness, Autosomal Dominant 31
Deafness, Autosomal Dominant 33
Deafness, Autosomal Dominant 36
Deafness, Autosomal Dominant 3a
Deafness, Autosomal Dominant 3b
Deafness, Autosomal Dominant 40
Deafness, Autosomal Dominant 41
Deafness, Autosomal Dominant 43
Deafness, Autosomal Dominant 44
Deafness, Autosomal Dominant 47
Deafness, Autosomal Dominant 48
Deafness, Autosomal Dominant 49
Deafness, Autosomal Dominant 4a
Deafness, Autosomal Dominant 4b
Deafness, Autosomal Dominant 5
Deafness, Autosomal Dominant 50
Deafness, Autosomal Dominant 51
Deafness, Autosomal Dominant 52
Deafness, Autosomal Dominant 53
Deafness, Autosomal Dominant 54
Deafness, Autosomal Dominant 56
Deafness, Autosomal Dominant 58
Deafness, Autosomal Dominant 59
Deafness, Autosomal Dominant 6
Deafness, Autosomal Dominant 64
Deafness, Autosomal Dominant 65
Deafness, Autosomal Dominant 66
Deafness, Autosomal Dominant 67
Deafness, Autosomal Dominant 68
Deafness, Autosomal Dominant 69
Deafness, Autosomal Dominant 7
Deafness, Autosomal Dominant 70
Deafness, Autosomal Dominant 71
Deafness, Autosomal Dominant 72
Deafness, Autosomal Dominant 73
Deafness, Autosomal Dominant 9
Deafness, Autosomal Recessive
Deafness, Autosomal Recessive 101
Deafness, Autosomal Recessive 102
Deafness, Autosomal Recessive 103
Deafness, Autosomal Recessive 104
Deafness, Autosomal Recessive 105
Deafness, Autosomal Recessive 106
Deafness, Autosomal Recessive 107
Deafness, Autosomal Recessive 108
Deafness, Autosomal Recessive 12
Deafness, Autosomal Recessive 13
Deafness, Autosomal Recessive 14
Deafness, Autosomal Recessive 15
Deafness, Autosomal Recessive 16
Deafness, Autosomal Recessive 17
Deafness, Autosomal Recessive 18a
Deafness, Autosomal Recessive 18b
Deafness, Autosomal Recessive 1a
Deafness, Autosomal Recessive 1b
Deafness, Autosomal Recessive 2
Deafness, Autosomal Recessive 20
Deafness, Autosomal Recessive 21
Deafness, Autosomal Recessive 22
Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 24
Deafness, Autosomal Recessive 25
Deafness, Autosomal Recessive 26
Deafness, Autosomal Recessive 27
Deafness, Autosomal Recessive 28
Deafness, Autosomal Recessive 29
Deafness, Autosomal Recessive 3
Deafness, Autosomal Recessive 30
Deafness, Autosomal Recessive 31
Deafness, Autosomal Recessive 32
Deafness, Autosomal Recessive 33
Deafness, Autosomal Recessive 35
Deafness, Autosomal Recessive 37
Deafness, Autosomal Recessive 38
Deafness, Autosomal Recessive 39
Deafness, Autosomal Recessive 40
Deafness, Autosomal Recessive 42
Deafness, Autosomal Recessive 44
Deafness, Autosomal Recessive 45
Deafness, Autosomal Recessive 46
Deafness, Autosomal Recessive 47
Deafness, Autosomal Recessive 48
Deafness, Autosomal Recessive 49
Deafness, Autosomal Recessive 5
Deafness, Autosomal Recessive 51
Deafness, Autosomal Recessive 53
Deafness, Autosomal Recessive 55
Deafness, Autosomal Recessive 59
Deafness, Autosomal Recessive 6
Deafness, Autosomal Recessive 61
Deafness, Autosomal Recessive 62
Deafness, Autosomal Recessive 63
Deafness, Autosomal Recessive 65
Deafness, Autosomal Recessive 66
Deafness, Autosomal Recessive 67
Deafness, Autosomal Recessive 68
Deafness, Autosomal Recessive 7
Deafness, Autosomal Recessive 70
Deafness, Autosomal Recessive 71
Deafness, Autosomal Recessive 74
Deafness, Autosomal Recessive 76
Deafness, Autosomal Recessive 77
Deafness, Autosomal Recessive 79
Deafness, Autosomal Recessive 8
Deafness, Autosomal Recessive 83
Deafness, Autosomal Recessive 84a
Deafness, Autosomal Recessive 84b
Deafness, Autosomal Recessive 85
Deafness, Autosomal Recessive 86
Deafness, Autosomal Recessive 88
Deafness, Autosomal Recessive 89
Deafness, Autosomal Recessive 9
Deafness, Autosomal Recessive 91
Deafness, Autosomal Recessive 93
Deafness, Autosomal Recessive 96
Deafness, Autosomal Recessive 97
Deafness, Autosomal Recessive 98
Deep Corneal Vascularisation
Dermato-Cardio-Skeletal Syndrome, Borrone Type
Dextrocardia
Dextrocardia with Situs Inversus
Dextro-Looped Transposition of the Great Arteries
Diabetic Angiopathy
Diastolic Heart Failure
Dieulafoy Lesion
Diffuse Lymphatic Malformation
Diffuse Neonatal Hemangiomatosis
Dilated Cardiomyopathy
Dilated Cardiomyopathy 1t
Discrete Fibromuscular Subaortic Stenosis
Discrete Subaortic Stenosis
Distichiasis with Congenital Anomalies of the Heart and Peripheral Vasculature
Dmd-Related Dilated Cardiomyopathy
Double-Orifice Mitral Valve
Double Outlet Left Ventricle
Double Outlet Right Ventricle with Atrioventricular Septal Defect, Pulmonary Stenosis, Heterotaxy
Double Outlet Right Ventricle with Non-Committed Subpulmonary Ventricular Septal Defect
Double Outlet Right Ventricle with Subaortic or Doubly Committed Ventricular Septal Defect with Pulmonary Stenosis
Down Syndrome
Doxorubicin Induced Cardiomyopathy
Dressler's Syndrome
Drug-Induced Vasculitis
Dural Sinus Malformation
Dysphagia Lusoria
Eales Disease
Ebstein Anomaly
Eclampsia
Ectasia of the Left Atrial Appendage
Ectasia of the Right Atrial Appendage
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema
Ectopia Cordis
Ectrodactyly Cardiopathy Dysmorphism
Ehlers-Danlos Syndrome, Cardiac Valvular Type
Ehlers-Danlos Syndrome, Musculocontractural Type, 1
Ehlers-Danlos Syndrome, Musculocontractural Type, 2
Ehlers-Danlos Syndrome, Vascular-Like Type
Ehlers-Danlos Syndrome, Vascular Type
Ellis-Van Creveld Syndrome
Emery-Dreifuss Muscular Dystrophy
Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive
Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant
Emery-Dreifuss Muscular Dystrophy, Dominant Type
Encephalopathy, Axonal, with Necrotizing Myopathy, Cardiomyopathy, and Cataracts
Encircling Double Aortic Arch
Endocardial Fibroelastosis
Endocarditis
Endocardium Cancer
Endocardium Disease
Endomyocardial Fibrosis
Eosinophilic Granulomatosis with Polyangiitis
Epicardium Cancer
Epicardium Lipoma
Epithelioid Hemangioendothelioma
Erythema Elevatum Diutinum
Erythrokeratodermia-Cardiomyopathy Syndrome
Erythromelalgia
Esophageal Varix
Extracranial Carotid Artery Aneurysm
Extrinsic Cardiomyopathy
Familial Abdominal Aortic Aneurysm
Familial Atrial Fibrillation
Familial Bicuspid Aortic Valve
Familial Deafness
Familial Hyperaldosteronism
Familial Hypertension
Familial Idiopathic Basal Ganglia Calcification
Familial Idiopathic Dilatation of the Right Atrium
Familial Isolated Arrhythmogenic Right Ventricular Dysplasia
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form
Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form
Familial Isolated Dilated Cardiomyopathy
Familial Isolated Restrictive Cardiomyopathy
Familial Long Qt Syndrome
Familial Partial Lipodystrophy
Familial Partial Lipodystrophy Due to Akt2 Mutations
Familial Patent Arterial Duct
Familial Short Qt Syndrome
Familial Sick Sinus Syndrome
Fatal Infantile Cytochrome C Oxidase Deficiency
Fatal Infantile Encephalocardiomyopathy
Fatal Infantile Hypertrophic Cardiomyopathy Due to Mitochondrial Complex I Deficiency
Femoral Vein Thrombophlebitis
Fibro-Adipose Vascular Anomaly
Fiedler's Myocarditis
First-Degree Atrioventricular Block
Foix-Alajouanine Syndrome
Frontonasal Arteriovenous Malformation
Gastric Antral Vascular Ectasia
Gastroesophageal Junction Adenocarcinoma
Gaucher's Disease
Gaucher Disease - Ophthalmoplegia - Cardiovascular Calcification
Gaucher Disease, Type I
Gaucher Disease, Type Ii
Gaucher Disease, Type Iii
Gaucher Disease, Type Iiic
Generalized Atherosclerosis
Genuine Diffuse Phlebectasia
German Syndrome
Glomuvenous Malformations
Glycogen Storage Disease
Glycogen Storage Disease Ia
Glycogen Storage Disease Ib
Glycogen Storage Disease Ic
Glycogen Storage Disease Ii
Glycogen Storage Disease Iii
Glycogen Storage Disease Iv
Glycogen Storage Disease Ix
Glycogen Storage Disease Ixa
Glycogen Storage Disease Ixb
Glycogen Storage Disease Ixc
Glycogen Storage Disease of Heart, Lethal Congenital
Glycogen Storage Disease Type 0
Glycogen Storage Disease, Type Ixd
Glycogen Storage Disease V
Glycogen Storage Disease Vi
Glycogen Storage Disease Vii
Glycogen Storage Disease Viii
Glycogen Storage Disease X
Glycogen Storage Disease Xii
Glycogen Storage Disease Xiii
Glycogen Storage Disease Xv
Goodpasture Syndrome
Granulomatous Angiitis
Hadziselimovic Syndrome
Heart Aneurysm
Heart Block, Congenital
Heart Cancer
Heart Conduction Disease
Heart Disease
Heart Fibrosarcoma
Heart-Hand Syndrome, Slovenian Type
Heart-Hand Syndrome, Spanish Type
Heart Leiomyosarcoma
Heart Lipoma
Heart Lymphoma
Heart Malignant Hemangiopericytoma
Heart Sarcoma
Heart Septal Defect
Hellp Syndrome
Hemangioblastoma
Hemangioma, Capillary Infantile
Hemihyperplasia-Multiple Lipomatosis Syndrome
Hemopericardium
Hemophilia a with Vascular Abnormality
Hemorrhoid
Hennekam Syndrome
Henoch-Schoenlein Purpura
Hepatic Infarction
Hepatic Vascular Disease
Hepatic Veno-Occlusive Disease
Hereditary Hemorrhagic Telangiectasia
Hereditary Paraganglioma-Pheochromocytoma Syndromes
Hereditary Vascular Retinopathy
Heterotaxy, Visceral, 2, Autosomal
Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 4, Autosomal
Heterotaxy, Visceral, 5, Autosomal
Heterotaxy, Visceral, 6, Autosomal
Heterotaxy, Visceral, 7, Autosomal
Heterotaxy, Visceral, 8, Autosomal
Histoplasmosis Pericarditis
Hughes-Stovin Syndrome
Hyperaldosteronism, Familial, Type I
Hyperaldosteronism, Familial, Type Ii
Hyperaldosteronism, Familial, Type Iii
Hyperaldosteronism, Familial, Type Iv
Hypersensitivity Vasculitis
Hypertaurinuric Cardiomyopathy
Hypertension and Brachydactyly Syndrome
Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy
Hypertension, Essential
Hypertension, Essential 1
Hypertension, Essential 2
Hypertension, Essential 3
Hypertension, Essential 4
Hypertension, Essential 5
Hypertension, Essential 6
Hypertension, Essential 7
Hypertension, Essential 8
Hypertensive Encephalopathy
Hypertensive Heart Disease
Hyperthyroidism, Familial Gestational
Hyperthyroidism, Nonautoimmune
Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy and Renal Tubular Disease Due to Mitochondrial Dna Mutation
Hypertrophic Cardiomyopathy Due to Intensive Athletic Training
Hypocomplementemic Urticarial Vasculitis
Hypogonadism Cardiomyopathy
Hypoplasia of the Mitral Valve Annulus
Hypoplastic Left Heart Syndrome
Hypoplastic Left Heart Syndrome 1
Hypoplastic Left Heart Syndrome 2
Hypoplastic Right Heart Syndrome
Hypotonia, Infantile, with Psychomotor Retardation
Idiopathic Dilatation of the Pulmonary Artery
Iliac Vein Thrombophlebitis
Immunodeficiency 23
Immunoglobulin a Vasculitis
Infections, Recurrent, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
Infectious Myocarditis
Infective Endocarditis
Inferior Myocardial Infarction
Inferior Vena Cava Interruption
Inferolateral Myocardial Infarct
Interatrial Communication
Intermediate Coronary Syndrome
Intermittent Claudication
Internal Carotid Agenesis
Internal Hemorrhoid
Interstitial Myocarditis
Intracranial Aneurysm
Intracranial Aneurysms Multiple Congenital Anomaly
Intracranial Arteriosclerosis
Intracranial Berry Aneurysm
Intracranial Embolism
Intracranial Hypertension, Idiopathic
Intracranial Sinus Thrombosis
Intracranial Thrombosis
Intracranial Vasospasm
Intramural Coronary Arterial Course
Intrinsic Cardiomyopathy
Inverse Klippel-Trénaunay Syndrome
Irvan Syndrome
Ischemia
Ischemic Heart Disease
Isolated Congenitally Uncorrected Transposition of the Great Arteries
Jervell and Lange-Nielsen Syndrome 1
Jervell and Lange-Nielsen Syndrome 2
Juvenile Temporal Arteritis
Juxtaposition of the Atrial Appendages
Kaposiform Hemangioendothelioma
Kaposiform Lymphangiomatosis
Kaposi Sarcoma
Kasznica Carlson Coppedge Syndrome
Kawasaki Disease
Kearns-Sayre Syndrome
Klippel-Trenaunay-Weber Syndrome
Kommerell Diverticulum
Kyphoscoliotic Heart Disease
Laryngotracheal Angioma
Lateral Medullary Syndrome
Lateral Myocardial Infarction
Lateral Sinus Thrombosis
Laubry-Pezzi Syndrome
Left Bundle Branch Hemiblock
Left Superior Vena Cava Persisting to Left-Sided Atrium
Left Ventricular Noncompaction
Left Ventricular Noncompaction 1
Left Ventricular Noncompaction 10
Left Ventricular Noncompaction 2
Left Ventricular Noncompaction 7
Left Ventricular Noncompaction 8
Leigh Syndrome
Lemierre's Syndrome
Leopard Syndrome
Leopard Syndrome 1
Leopard Syndrome 2
Leopard Syndrome 3
Levocardia
Liddle Syndrome
Limb Ischemia
Linear Skin Defects with Multiple Congenital Anomalies 1
Linear Skin Defects with Multiple Congenital Anomalies 2
Linear Skin Defects with Multiple Congenital Anomalies 3
Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules
Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy
Lipodystrophy, Familial Partial, Type 1
Lipodystrophy, Familial Partial, Type 2
Lipodystrophy, Familial Partial, Type 3
Lipodystrophy, Familial Partial, Type 4
Lipodystrophy, Familial Partial, Type 5
Lipodystrophy, Familial Partial, Type 6
Lipodystrophy, Partial, Acquired
Lissencephaly
Lissencephaly 1
Lissencephaly 2
Lissencephaly 3
Lissencephaly 4
Lissencephaly 5
Lissencephaly 8
Livedoid Vasculopathy
Lmna-Related Cardiocutaneous Progeria Syndrome
Lmna-Related Dilated Cardiomyopathy
Loeffler Endocarditis
Loeys-Dietz Syndrome 2
Loeys-Dietz Syndrome 3
Long Qt Syndrome
Long Qt Syndrome 1
Long Qt Syndrome 10
Long Qt Syndrome 11
Long Qt Syndrome 12
Long Qt Syndrome 13
Long Qt Syndrome 14
Long Qt Syndrome 15
Long Qt Syndrome 2
Long Qt Syndrome 3
Long Qt Syndrome 5
Long Qt Syndrome 6
Long Qt Syndrome 9
Lutembacher's Syndrome
Lymphangiectasia, Pulmonary, Congenital
Lymphangitis
Lymphedema and Cerebral Arteriovenous Anomaly
Lymphedema, Cardiac Septal Defects, and Characteristic Facies
Lymphedema-Hypoparathyroidism Syndrome
Lymphedema, Primary, with Myelodysplasia
Lymphocytic Vasculitis
Male Genital Organ Vascular Disease
Malignant Cardiac Germ Cell Tumor
Malignant Epithelioid Hemangioendothelioma
Malignant Essential Hypertension
Malignant Hypertension
Malignant Hypertensive Renal Disease
Malignant Renovascular Hypertension
Malignant Secondary Hypertension
Malposition of the Coronary Ostium
Mandibular Arteriovenous Malformation
Marantic Endocarditis
Marfan Syndrome
Maternally-Inherited Cardiomyopathy and Hearing Loss
Maxillary Arteriovenous Malformation
May-Thurner Syndrome
Meacham Syndrome
Median Arcuate Ligament Syndrome
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome
Megalocornea-Mental Retardation Syndrome
Mental Retardation and Distinctive Facial Features with or Without Cardiac Defects
Mental Retardation, Autosomal Dominant 10
Mental Retardation, Autosomal Dominant 11
Mental Retardation, Autosomal Dominant 13
Mental Retardation, Autosomal Dominant 18
Mental Retardation, Autosomal Dominant 19
Mental Retardation, Autosomal Dominant 20
Mental Retardation, Autosomal Dominant 21
Mental Retardation, Autosomal Dominant 22
Mental Retardation, Autosomal Dominant 23
Mental Retardation, Autosomal Dominant 24
Mental Retardation, Autosomal Dominant 26
Mental Retardation, Autosomal Dominant 27
Mental Retardation, Autosomal Dominant 29
Mental Retardation, Autosomal Dominant 30
Mental Retardation, Autosomal Dominant 31
Mental Retardation, Autosomal Dominant 32
Mental Retardation, Autosomal Dominant 33
Mental Retardation, Autosomal Dominant 34
Mental Retardation, Autosomal Dominant 35
Mental Retardation, Autosomal Dominant 36
Mental Retardation, Autosomal Dominant 38
Mental Retardation, Autosomal Dominant 39
Mental Retardation, Autosomal Dominant 40
Mental Retardation, Autosomal Dominant 41
Mental Retardation, Autosomal Dominant 42
Mental Retardation, Autosomal Dominant 43
Mental Retardation, Autosomal Dominant 44
Mental Retardation, Autosomal Dominant 45
Mental Retardation, Autosomal Dominant 46
Mental Retardation, Autosomal Dominant 47
Mental Retardation, Autosomal Dominant 48
Mental Retardation, Autosomal Dominant 49
Mental Retardation, Autosomal Dominant 50
Mental Retardation, Autosomal Dominant 51
Mental Retardation, Autosomal Dominant 52
Mental Retardation, Autosomal Dominant 53
Mental Retardation, Autosomal Dominant 54
Mental Retardation, Autosomal Dominant 56
Mental Retardation, Autosomal Dominant 7
Mental Retardation, Autosomal Recessive 14
Mental Retardation, Autosomal Recessive 15
Mental Retardation, Autosomal Recessive 16
Mental Retardation, Autosomal Recessive 18
Mental Retardation, Autosomal Recessive 19
Mental Retardation, Autosomal Recessive 2
Mental Retardation, Autosomal Recessive 23
Mental Retardation, Autosomal Recessive 24
Mental Retardation, Autosomal Recessive 25
Mental Retardation, Autosomal Recessive 27
Mental Retardation, Autosomal Recessive 28
Mental Retardation, Autosomal Recessive 29
Mental Retardation, Autosomal Recessive 30
Mental Retardation, Autosomal Recessive 31
Mental Retardation, Autosomal Recessive 33
Mental Retardation, Autosomal Recessive 35
Mental Retardation, Autosomal Recessive 36
Mental Retardation, Autosomal Recessive 37
Mental Retardation, Autosomal Recessive 38
Mental Retardation, Autosomal Recessive 39
Mental Retardation, Autosomal Recessive 40
Mental Retardation, Autosomal Recessive 41
Mental Retardation, Autosomal Recessive 42
Mental Retardation, Autosomal Recessive 43
Mental Retardation, Autosomal Recessive 44
Mental Retardation, Autosomal Recessive 45
Mental Retardation, Autosomal Recessive 46
Mental Retardation, Autosomal Recessive 47
Mental Retardation, Autosomal Recessive 48
Mental Retardation, Autosomal Recessive 49
Mental Retardation, Autosomal Recessive 5
Mental Retardation, Autosomal Recessive 50
Mental Retardation, Autosomal Recessive 51
Mental Retardation, Autosomal Recessive 52
Mental Retardation, Autosomal Recessive 53
Mental Retardation, Autosomal Recessive 54
Mental Retardation, Autosomal Recessive 55
Mental Retardation, Autosomal Recessive 56
Mental Retardation, Autosomal Recessive 57
Mental Retardation, Autosomal Recessive 58
Mental Retardation, Autosomal Recessive 59
Mental Retardation, Autosomal Recessive 60
Mental Retardation, Autosomal Recessive 61
Mental Retardation, X-Linked, Syndromic 13
Mental Retardation, X-Linked, Syndromic 17
Mental Retardation, X-Linked, Syndromic 32
Mental Retardation, X-Linked, Syndromic 33
Mental Retardation, X-Linked, Syndromic 34
Mental Retardation, X-Linked, Syndromic, 35
Mental Retardation, X-Linked, Syndromic 9
Mental Retardation, X-Linked, Syndromic, Wu Type
Mesenteric Vascular Occlusion
Mesoaxial Hexadactyly and Cardiac Malformation
Mesocardia
Microcephaly-Capillary Malformation Syndrome
Microcephaly-Cardiomyopathy
Microcephaly, Congenital Heart Disease, Unilateral Renal Agenesis, and Hyposegmented Lungs
Microcornea Posterior Megalolenticonus Persistent Fetal Vasculature Coloboma
Microcystic Lymphatic Malformation
Microphthalmia, Syndromic 1
Microphthalmia, Syndromic 10
Microphthalmia, Syndromic 11
Microphthalmia, Syndromic 12
Microphthalmia, Syndromic 13
Microphthalmia, Syndromic 2
Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 4
Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 6
Microphthalmia, Syndromic 8
Microphthalmia, Syndromic 9
Microscopic Polyangiitis
Middle Cerebral Artery Infarction
Mild Pre-Eclampsia
Mitochondrial Complex Iv Deficiency
Mitochondrial Complex V Deficiency, Nuclear Type 2
Mitochondrial Dna Depletion Syndrome 12a , Autosomal Dominant
Mitochondrial Dna Depletion Syndrome 12b , Autosomal Recessive
Mitochondrial Dna Depletion Syndrome 14
Mitochondrial Phosphate Carrier Deficiency
Mitral Atresia
Mitral Valve Agenesis
Mitral Valve Disease
Mitral Valve Insufficiency
Mitral Valve Prolapse 1
Mitral Valve Prolapse 2
Mitral Valve Prolapse 3
Mitral Valve Prolapse, Familial, Autosomal Dominant
Mitral Valve Stenosis
Mixed Connective Tissue Disease
Mixed Cryoglobulinemia Type Iii
Mixed Cystic Lymphatic Malformation
Mobitz Type Ii Atrioventricular Block
Monckeberg Arteriosclerosis
Moyamoya Disease 1
Moyamoya Disease 2
Moyamoya Disease 3
Moyamoya Disease 5
Mullerian Derivatives, Persistence of, with Lymphangiectasia and Postaxial Polydactyly
Multifocal Lymphangioendotheliomatosis with Thrombocytopenia
Multiple Enchondromatosis, Maffucci Type
Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects
Multisystemic Smooth Muscle Dysfunction Syndrome
Muscular Dystrophy
Muscular Dystrophy, Congenital, 1b
Muscular Dystrophy, Congenital Merosin-Deficient, 1a
Musculocontractural Ehlers-Danlos Syndrome
Myocardial Infarction
Myocardial Infarction 2
Myocardial Stunning
Myocarditis
Myocardium Cancer
Myofibrillar Myopathy
Myopathy, Myofibrillar, 1
Myopathy, Myofibrillar, 2
Myopathy, Myofibrillar, 3
Myopathy, Myofibrillar, 4
Myopathy, Myofibrillar, 5
Myopathy, Myofibrillar, 6
Myopathy, Myofibrillar, 7
Myopathy, Myofibrillar, 8
Myotonia Congenita
Myotonia Congenita, Autosomal Dominant
Myotonia Congenita, Autosomal Recessive
Naxos Disease
Neonatal Marfan Syndrome
Nephrosclerosis
Neurofibromatosis-Noonan Syndrome
Neurofibromatosis, Type I
Neurofibromatosis, Type Ii
Neutral Lipid Storage Disease with Myopathy
Non-Involuting Congenital Hemangioma
Nonsyndromic Deafness
Noonan Syndrome 1
Noonan Syndrome 10
Noonan Syndrome 2
Noonan Syndrome 3
Noonan Syndrome 4
Noonan Syndrome 5
Noonan Syndrome 6
Noonan Syndrome 7
Noonan Syndrome 8
Noonan Syndrome 9
Noonan Syndrome-Like Disorder with Loose Anagen Hair 1
Noonan Syndrome-Like Disorder with Loose Anagen Hair 2
Noonan Syndrome-Like Disorder with or Without Juvenile Myelomonocytic Leukemia
Noonan Syndrome with Multiple Lentigines
Nuchal Bleb, Familial
Nutmeg Liver
Occlusion Precerebral Artery
Olivopontocerebellar Atrophy
Olivopontocerebellar Atrophy Ii, Autosomal Recessive
Olivopontocerebellar Atrophy V
Omphalocele-Diaphragmatic Hernia-Cardiovascular Anomalies-Radial Ray Defect Syndrome
Orthostatic Intolerance
Pancytopenia and Occlusive Vascular Disease
Parachute Tricuspid Valve
Parkes Weber Syndrome
Partial Arterial Retinal Occlusion
Partial Atrioventricular Canal
Partially Involuting Congenital Hemangioma
Partial of Retinal Vein Occlusion
Patent Ductus Arteriosus 1
Patent Ductus Arteriosus 2
Patent Ductus Arteriosus 3
Patent Ductus Arteriosus and Bicuspid Aortic Valve with Hand Anomalies
Patent Foramen Ovale
Pediatric Arterial Ischemic Stroke
Peliosis Hepatis
Pelvic Varices
Perianal Hematoma
Pericardial Effusion
Pericardial Effusion, Chronic
Pericardial Mesothelioma
Pericarditis
Pericardium Cancer
Peripartum Cardiomyopathy
Peripheral Artery Disease
Peripheral Vascular Disease
Periventricular Nodular Heterotopia
Periventricular Nodular Heterotopia 1
Periventricular Nodular Heterotopia 6
Periventricular Nodular Heterotopia 7
Persistent Eustachian Valve
Persistent Fetal Circulation Syndrome
Persistent Fifth Aortic Arch
Persistent Hyperplastic Primary Vitreous
Persistent Hyperplastic Primary Vitreous, Autosomal Dominant
Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
Persistent Left Superior Vena Cava Connecting to the Left-Sided Atrium
Peters-Plus Syndrome
Phacomatosis Pigmentovascularis
Piepkorn Karp Hickok Syndrome
Placental Insufficiency
Pleuro-Pericardial Cyst
Polyarteritis Nodosa
Polyarteritis Nodosa, Childhood-Onset
Polyneuropathy in Collagen Vascular Disease
Polyvalvular Heart Disease Syndrome
Portal Hypertension
Portal Hypertension Due to Infrahepatic Block
Portal Vein, Cavernous Transformation of
Portal Vein Thrombosis
Posterior Cerebral Artery Infarction
Posterior Myocardial Infarction
Posteroinferior Myocardial Infarction
Posterolateral Myocardial Infarction
Post-Infectious Myocarditis
Postinfectious Vasculitis
Post-Thrombotic Syndrome
Pre-Eclampsia
Premature Closure of the Arterial Duct
Prepapillary Vascular Loops
Priapism
Primary Angiitis of the Central Nervous System
Primary Intralymphatic Angioendothelioma
Primary Polyarteritis Nodosa
Primitive Portal Vein Thrombosis
Prinzmetal's Variant Angina
Progressive Familial Heart Block
Progressive Familial Heart Block, Type Ia
Progressive Familial Heart Block, Type Ib
Progressive Familial Heart Block, Type Ii
Proliferative Vasculopathy and Hydranencephaly-Hydrocephaly Syndrome
Proteus-Like Syndrome
Proteus Syndrome
Pseudo-Gaucher Disease
Pseudohypoaldosteronism
Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type Iia
Pseudohypoaldosteronism, Type Iib
Pseudohypoaldosteronism, Type Iic
Pseudohypoaldosteronism, Type Iid
Pseudohypoaldosteronism, Type Iie
Pseudoxanthoma Elasticum
Puerperal Pulmonary Embolism
Pulmonary Arterio-Veinous Fistula
Pulmonary Arteriovenous Fistulas
Pulmonary Artery Choriocarcinoma
Pulmonary Artery Coming from Patent Ductus Arteriosus
Pulmonary Artery Coming from the Aorta
Pulmonary Artery Hypoplasia
Pulmonary Artery Leiomyosarcoma
Pulmonary Atresia with Intact Ventricular Septum
Pulmonary Atresia with Ventricular Septal Defect
Pulmonary Branches Stenosis
Pulmonary Embolism
Pulmonary Embolism and Infarction
Pulmonary Hypertension
Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis
Pulmonary Hypertension, Primary, 1
Pulmonary Hypertension, Primary, 2
Pulmonary Hypertension, Primary, 3
Pulmonary Hypertension, Primary, 4
Pulmonary Hypertension, Primary, Autosomal Recessive
Pulmonary Subvalvular Stenosis
Pulmonary Supravalvular Stenosis
Pulmonary Valve Agenesis-Tetralogy of Fallot-Absence of Ductus Arteriosus Syndrome
Pulmonary Valve Agenesis-Ventricular Septal Defect-Persistent Ductus Arteriosus Syndrome
Pulmonary Valve Disease
Pulmonary Valve Insufficiency
Pulmonary Valve Stenosis
Pulmonary Vein Leiomyosarcoma
Pulmonary Vein Stenosis
Pulmonary Venoocclusive Disease
Pulmonary Venoocclusive Disease 1, Autosomal Dominant
Pulmonary Venoocclusive Disease 2, Autosomal Recessive
Pulmonic Stenosis
Pure Autonomic Failure
Rapidly Involuting Congenital Hemangioma
Raynaud Disease
Renal Artery Atheroma
Renal Artery Disease
Renal Artery Obstruction
Renal Failure, Progressive, with Hypertension
Renal Hypertension
Renal Nutcracker Syndrome
Renovascular Hypertension
Restrictive Cardiomyopathy
Retiform Hemangioendothelioma
Retinal Arterial Macroaneurysm with Supravalvular Pulmonic Stenosis
Retinal Arteries, Tortuosity of
Retinal Artery Occlusion
Retinal Capillary Malformation
Retinal Hemangioblastoma
Retinal Vascular Disease
Retinal Vascular Occlusion
Retinal Vasculitis
Retinal Vein Occlusion
Rheumatic Disease
Rheumatic Fever
Rheumatic Heart Disease
Rheumatic Myocarditis
Rheumatic Pulmonary Valve Disease
Rheumatoid Vasculitis
Right Aortic Arch
Right Atrial Isomerism
Right Bundle Branch Block
Right Inferior Vena Cava Connecting to Left-Sided Atrium
Right Superior Vena Cava Connecting to Left-Sided Atrium
Right Ventricular Hypoplasia, Isolated
Ruvalcaba Churesigaew Myhre Syndrome
Sagittal Sinus Thrombosis
Salih Myopathy
Secondary Polyarteritis Nodosa
Second-Degree Atrioventricular Block
Segmental Outgrowth-Lipomatosis-Arteriovenous Malformation-Epidermal Nevus Syndrome
Sengers Syndrome
Septal Myocardial Infarction
Septic Myocarditis
Severe Pre-Eclampsia
Shone Complex
Short Qt Syndrome
Short Qt Syndrome 1
Short Qt Syndrome 2
Short Qt Syndrome 3
Short Stature, Developmental Delay, and Congenital Heart Defects
Short Syndrome
Shwartzman Phenomenon
Sialadenitis
Sick Sinus Syndrome
Sick Sinus Syndrome 1
Sick Sinus Syndrome 2
Sick Sinus Syndrome 3
Silent Myocardial Infarction
Single-Organ Polyarteritis Nodosa
Sinoatrial Node Disease
Sneddon Syndrome
Spindle Cell Hemangioma
Spine Rigid Cardiomyopathy
Splenic Artery Aneurysm
Splenoportal Vascular Anomalies
Stenosis or Atresia of the Coronary Ostium
Sternal Cyst Vascular Anomalies
Sternal Malformation Vascular Dysplasia Associatio
Sting-Associated Vasculopathy, Infantile-Onset
Sting-Associated Vasculopathy with Onset in Infancy
Stork Bite
Straddling and/or Overriding Mitral Valve
Straddling or Overriding Tricuspid Valve
Strictly Posterior Acute Myocardial Infarction
Stroke, Ischemic
Sturge-Weber Syndrome
Subacute Bacterial Endocarditis
Subaortic Course of Innominate Vein
Subaortic Stenosis, Membranous
Subclavian Artery Aneurysm
Subendocardial Infarction Acute Myocardial Infarction
Subendocardial Myocardial Infarction
Subpulmonary Stenosis
Subvalvular Aortic Stenosis
Superior Mesenteric Artery Syndrome
Superior Vena Cava Angiosarcoma
Superior Vena Cava Leiomyosarcoma
Supine Hypotensive Syndrome
Supravalvular Aortic Stenosis
Susac Syndrome
Sydenham Chorea
Systemic Capillary Leak Syndrome
Systemic Polyarteritis Nodosa
Systolic Heart Failure
Takayasu Arteritis
Tarp Syndrome
Telangiectasia, Hereditary Hemorrhagic, Type 1
Telangiectasia, Hereditary Hemorrhagic, Type 2
Telangiectasia, Hereditary Hemorrhagic, Type 3
Telangiectasia, Hereditary Hemorrhagic, Type 4
Telangiectasia, Hereditary Hemorrhagic, Type 5
Telangiectasis
Temporal Arteritis
Tetralogy of Fallot
Tetralogy of Fallot Syndrome, Autosomal Recessive
Third-Degree Atrioventricular Block
Thoracic Outlet Syndrome
Thrombophlebitis
Thrombophlebitis Migrans
Thrombosis
Tmem70 Defect
Total Anomalous Pulmonary Venous Return 1
Toxic Myocarditis
Transient Cerebral Ischemia
Transient Pseudohypoaldosteronism
Transient Retinal Arterial Occlusion
Transmitted_by
Transposition of the Great Arteries, Dextro-Looped 1
Transposition of the Great Arteries, Dextro-Looped 3
Tricuspid Atresia
Tricuspid Valve Agenesis
Tricuspid Valve Disease
Tricuspid Valve Insufficiency
Tricuspid Valve Prolapse
Tricuspid Valve Stenosis
Tubular Renal Disease-Cardiomyopathy Syndrome
Tunnel Subaortic Stenosis
Type Ii Mixed Cryoglobulinemia
Unclassified Vasculitis
Univentricular Heart
Univentricular Heart with Single Atrio-Ventricular Valve
Varicocele
Varicose Veins
Vascular Cancer
Vascular Dementia
Vascular Disease
Vascular Erectile Tumor
Vascular Helix of Umbilical Cord
Vascular Hemostatic Disease
Vascular Hyalinosis
Vascular Malformation, Primary Intraosseous
Vascular Myelopathy
Vascular Skin Disease
Vasculitis
Vasculitis, Lymphocytic, Cutaneous Small Vessel
Vasculitis, Lymphocytic, Nodular
Vasculitis Syndromes of the Central and Peripheral Nervous Systems
Vasculogenic Impotence
Vasculopathy, Retinal, with Cerebral Leukodystrophy
Vein Disease
Vein of Galen Aneurysm
Veins, Pattern of, on Anterior Thorax
Velocardiofacial Syndrome
Venous Insufficiency
Venous Malformations, Multiple Cutaneous and Mucosal
Venous Thoracic Outlet Syndrome
Venous Tributary Occlusion of Retina
Ventricular Septal Defect
Ventricular Septal Defect 1
Ventricular Septal Defect 2
Ventricular Septal Defect 3
Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy
Ventricular Tachycardia, Catecholaminergic Polymorphic, 2
Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
Ventricular Tachycardia, Catecholaminergic Polymorphic, 4
Venular Insufficiency, Systemic
Verrucous Hemangioma
Vertebral Artery Insufficiency
Vertebral Artery Occlusion
Vertebrobasilar Insufficiency
Visceral Calciphylaxis
Visceral Heterotaxy
Von Hippel-Lindau Syndrome
Von Willebrand's Disease
Wegener Granulomatosis
White Forelock with Malformations
Williams-Beuren Syndrome
Wolff-Parkinson-White Syndrome
Wyburn Mason's Syndrome
Yellow Nail Syndrome |
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