| Diseases |
Alias |
|
| Nemaline Myopathy 5 |
|
Amish Nemaline Myopathy
|
NEM5
|
|
Anm
|
Nemaline Myopathy, Amish Type
|
|
Nemaline Myopathy 5, Amish Type
|
Nemaline Myopathy, Caused By Mutation In The Troponin T1 Gene
|
|
Nemaline Myopathy, Type 5
|
Nemaline Myopathy Amish Type
|
|
Tnnt1-Related Nemaline Myopathy
|
Myopathy, Nemaline, Type 5
|
|
|
| Nemaline Myopathy |
|
Rod Myopathy
|
Nemaline Body Disease
|
|
Nemaline Rod Myopathy
|
Myopathies, Nemaline
|
|
Nm
|
Nemaline Rod Disease
|
|
Rod Body Disease
|
Rod-Body Myopathy
|
|
Myopathy, Nemaline
|
Congenital Rod Disease
|
|
Nem
|
Nemaline Bodies
|
|
Myopathies Nemaline
|
|
|
| Myopathy |
|
Muscular Diseases
|
Myopathies
|
|
|
| Acute Anterolateral Myocardial Infarction |
|
Acute Myocardial Infarction Of Anterolateral Wall
|
|
|
| Pectus Carinatum |
|
Carinatum Deformity Of The Chest
|
|
|
| Cataract 10, Multiple Types |
|
Cataract 10 Multiple Types
|
CTRCT10
|
|
Cataract, Congenital Zonular, With Sutural Opacities
|
Cczs
|
|
Congenital Zonular Cataract With Sutural Opacities
|
Cataract, Congenital, Zonular With Sutural Opacities
|
|
Cataract, Type 10, Multiple Types
|
|
|
| Pulmonary Embolism |
|
Pulmonary Artery Embolism
|
Pulmonary Embolus
|
|
Pulmonary Emboli
|
|
|
| Left Bundle Branch Hemiblock |
|
Left Bundle Branch Block
|
Left Bundle-Branch Block
|
|
|
| Inferior Myocardial Infarction |
|
Inferior Wall Myocardial Infarction
|
|
|
| Congenital Structural Myopathy |
|
|
| Myocarditis |
|
Myocardial Inflammation
|
Inflammatory Cardiomyopathy
|
|
|
| Acute Myocarditis |
|
|
| Hypertrophic Cardiomyopathy |
|
Hypertrophic Obstructive Cardiomyopathy
|
Cardiomyopathy, Hypertrophic
|
|
Cardiomyopathy Hypertrophic Obstructive
|
Cardiomyopathy, Hypertrophic, Familial
|
|
Idiopathic Myocardial Hypertrophy
|
Idiopathic Hypertrophic Cardiomyopathy
|
|
Obstructive Idiopathic Hypertrophic Cardiomyopathy
|
Obstructive Cardiomyopathy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Muscular Subaortic Stenosis
|
|
Hypertrophic Obstructive Subaortic Stenosis
|
|
|
| Intermediate Coronary Syndrome |
|
Unstable Angina
|
Angina At Rest
|
|
Anginal Chest Pain At Rest
|
Impending Infarction
|
|
Preinfarction Angina
|
Worsening Angina
|
|
Angina, Unstable
|
Myocardial Preinfarction Syndrome
|
|
Angina Unstable
|
Crescendo Angina
|
|
Angina Decubitus
|
Acute Coronary Insufficiency
|
|
Unstable Angina Pectoris
|
Preinfarctional Angina Pectoris
|
|
Worsening Effort Angina
|
Preinfarction Syndrome
|
|
Unstable Angina Pectoris Syndrome
|
Unstable Anginal Attack
|
|
Unstable Cardiac Angina
|
Unstable Chest Angina
|
|
Unstable Heart Angina
|
De Novo Effort Angina Pectoris
|
|
Crescendo Angina Pectoris
|
Ua - [Unstable Angina]
|
|
|
| Arthrogryposis, Distal, Type 2b2 |
|
DA2B2
|
Distal Arthrogryposis Type 2b2
|
|
Arthrogryposis, Distal, 2b2
|
|
|
| Autosomal Recessive Nonsyndromic Deafness 32 |
|
Deafness, Autosomal Recessive 32
|
Autosomal Recessive Deafness 105
|
|
Autosomal Recessive Deafness 32
|
Dfnb32
|
|
Hearing Impairment Infertile Male Syndrome
|
Hiims
|
|
Deafness, Autosomal Recessive, Type 32
|
|
|
| Cardiomyopathy, Dilated, 2a |
|
Dilated Cardiomyopathy 2a
|
CMD2A
|
|
Cardiomyopathy, Dilated, Autosomal Recessive
|
Cardiomyopathy, Congestive, Autosomal Recessive
|
|
Cardiomyopathy, Dilated 2a
|
Cardiomyopathy, Dilated, Type 2a
|
|
Autosomal Recessive Dilated Cardiomyopathy
|
|
|
| Cardiomyopathy, Dilated, 1ff |
|
Dilated Cardiomyopathy 1ff
|
CMD1FF
|
|
Cardiomyopathy, Dilated 1ff
|
Cardiomyopathy, Dilated, Type 1ff
|
|
|
| Mitral Valve Insufficiency |
|
Mitral Regurgitation
|
Congenital Insufficiency Of Mitral Valve
|
|
Congenital Mitral Insufficiency
|
Congenital Mitral Regurgitation
|
|
Mitral Valve Incompetence
|
Mitral Valve Regurgitation
|
|
Mr - [Mitral Regurgitation]
|
Mi - [Mitral Incompetence]
|
|
Mitral Valve Annular Incompetency
|
Congenital Mitral Valve Incompetence
|
|
Congenital Mitral Valve Insufficiency
|
Congenital Mitral Valve Regurgitation
|
|
Congenital Mitral Incompetence
|
|
|
| Immunoglobulin Light Chain Amyloidosis |
|
Al Amyloidosis
|
Primary Amyloidosis
|
|
Primary Systemic Amyloidosis
|
Light Chain Amyloidosis
|
|
Amyloidosis Al
|
Amyloidosis Primary Systemic
|
|
Primary Al Amyloidosis
|
Primary Systemic Al Amyloidosis
|
|
Systemic Al Amyloidsis
|
Systemic Al Amyloidosis
|
|
Light-Chain Amyloidosis
|
Alys Amyloidosis
|
|
Familial Amyloid Nephropathy Due To Lysozyme Variant
|
Familial Renal Amyloidosis Due To Lysozyme Variant
|
|
Hereditary Amyloid Nephropathy Due To Lysozyme Variant
|
Hereditary Renal Amyloidosis Due To Lysozyme Variant
|
|
Lysozyme Amyloidosis
|
Amyloidosis Primary
|
|
Immunoglobulin Deposition Disease
|
Immunoglobulinic Amyloidosis
|
|
Amyloid Al
|
|
|
| Coronary Artery Vasospasm |
|
Coronary Vasospasm
|
Coronary Artery Spasm
|
|
|
| Myocardial Stunning |
|
|
| Congenital Fiber-Type Disproportion |
|
Congenital Fiber Type Disproportion
|
Cftdm
|
|
Congenital Myopathy With Fiber Type Disproportion
|
Cftd
|
|
Congenital Fiber-Type Disproportion Myopathy
|
Fiber-Type Disproportion Myopathy, Congenital
|
|
Myopathy, Congenital With Fiber-Type Disproportion
|
|
|
| Nonobstructive Coronary Artery Disease |
|
Non-Cad
|
Non-Obstructive Coronary Artery Disease
|
|
|
| Extrinsic Cardiomyopathy |
|
|
| Pericardium Disease |
|
|
| Tricuspid Valve Insufficiency |
|
Tricuspid Regurgitation
|
Tricuspid Valve Regurgitation
|
|
Tricuspid Incompetence
|
Tr - [Tricuspid Regurgitation]
|
|
Tricuspid Valve Incompetency
|
Tricuspid Valve Annular Incompetency
|
|
|
| Pericardial Effusion |
|
Noninflammatory Pericardial Effusion
|
Pericardium Effusion
|
|
|
| Mitral Valve Disease |
|
Chronic Rheumatic Mitral Valve
|
Rheumatic Mitral Insufficiency
|
|
Disease Of Mitral Valve
|
Mitral Rh Valve Dis.
|
|
Rheumatic Disease Of Mitral Valve
|
Rheumatic Mitral Valve Changes
|
|
Rheumatic Mitral Valve Incompetence
|
Rheumatic Mitral Valve Regurgitation
|
|
Abnormality Of The Mitral Valve
|
Diseases Of Mitral Valve
|
|
Rheumatic Mitral Regurgitation
|
|
|
| Myopathy, Centronuclear, 1 |
|
Autosomal Dominant Centronuclear Myopathy
|
CNM1
|
|
Centronuclear Myopathy 1
|
Ad-Cnm
|
|
Myopathy, Centronuclear, Autosomal Dominant
|
Myotubular Myopathy, Autosomal Dominant
|
|
Centronuclear Myopathy, Autosomal, Modifier Of
|
Autosomal Dominant Myotubular Myopathy
|
|
Dnm2-Related Centronuclear Myopathy
|
Centronuclear Myopathy Autosomal Dominant
|
|
Myopathies, Structural, Congenital
|
Myopathy, Centronuclear, Type 1
|
|
|
| Gas Gangrene |
|
Myonecrosis
|
Gas Bacillus Infection
|
|
Gas Gangrene Due To Clostridia
|
Clostridial Myonecrosis
|
|
Clostridial Cellulitis
|
|
|
| Combined Oxidative Phosphorylation Deficiency 33 |
|
|
| 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
|
|
|
| Tricuspid Valve Disease |
|
Rheumatic Tricuspid Valve Disease
|
Disease Of Tricuspid Valve
|
|
Rh. Tricuspid Valve Disease
|
Rheumatic Disease Of Tricuspid Valve
|
|
Tricuspid Disease
|
Tricuspid Valve Disorder
|
|
|
| Batten-Turner Congenital Myopathy |
|
Congenital Myopathy
|
Batten Turner Congenital Myopathy
|
|
Myopathy Congenital
|
Myopathy, Congenital
|
|
Myotonia Congenita
|
Benign Congenital Myopathy
|
|
|
| Combined Oxidative Phosphorylation Deficiency 37 |
|
|
| Pulmonary Artery Disease |
|
Abnormality Of The Pulmonary Artery
|
|
|
| Lipoprotein Quantitative Trait Locus |
|
Coronary Artery Disease
|
Coronary Artery Anomaly
|
|
Coronary Artery Disease, Susceptibility To
|
Myocardial Ischemia
|
|
Congenital Anomaly Of Coronary Artery
|
Coronary Arteriosclerosis
|
|
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
|
|
|
| Charcot-Marie-Tooth Disease |
|
Cmt
|
Hmsn
|
|
Hereditary Motor And Sensory Neuropathy
|
Pma
|
|
Cmt - Charcot-Marie-Tooth Disease
|
Charcot Marie Tooth Disease
|
|
Charcot-Marie-Tooth Hereditary Neuropathy
|
Charcot-Marie-Tooth Syndrome
|
|
Peroneal Muscular Atrophy
|
Hereditary Motor And Sensory Neuropathies
|
|
|
| Distal Arthrogryposis |
|
Arthrogryposis Multiplex Congenita
|
Arthrogryposis
|
|
Congenital Multiple Arthrogryposis
|
Congenital Arthromyodysplasia
|
|
Fibrous Ankylosis Of Multiple Joints
|
Guerin-Stern Syndrome
|
|
Guérin-Stern Syndrome
|
Myodystrophia Fetalis Deformans
|
|
Otto Syndrome
|
Rocher-Sheldon Syndrome
|
|
Rossi Syndrome
|
Amc
|
|
Multiple Congenital Arthrogryposis
|
Arthrogryposis Syndrome
|
|
Arthrogryposis, Distal
|
Distal Arthrogryposis Syndrome
|
|
Freeman-Sheldon Syndrome
|
Arthrogryposis, Distal, Type 2b
|
|
Congenital Multiplex Arthrogryposis
|
Amyoplasia Congenita
|
|
Congenital Amyoplasia
|
Amc - [Arthrogryposis Multiplex Congenita]
|
|
|
| Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome |
|
Jacobs Syndrome
|
Arthropathy-Camptodactyly Syndrome
|
|
Pericarditis-Arthropathy-Camptodactyly Syndrome
|
Xyy Syndrome
|
|
Pac Syndrome
|
Cacp Syndrome
|
|
CACP
|
Fibrosing Serositis, Familial
|
|
Camptodactyly-Arthropathy-Pericarditis Syndrome
|
Cap Syndrome
|
|
47, Xyy Syndrome
|
47,Xyy Syndrome
|
|
Double Y Syndrome
|
Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis Syndrome
|
|
Hypertrophic Synovitis, Congenital Familial
|
Congenital Familial Hypertrophic Synovitis
|
|
Xyy Karyotype
|
Y Disomy
|
|
Yy Syndrome
|
Familial Fibrosing Serositis
|
|
Disomy Y
|
Double Y
|
|
Camptodactyly Arthropathy Coxa Vara Pericarditis Syndrome
|
Arthropathy Camptodactyly Syndrome
|
|
Camptodactyly Arthropathy Pericarditis Syndrome
|
Pericarditis Arthropathy Camptodactyly Syndrome
|
|
Jacob'S Syndrome
|
47,Xyy
|
|
Cdags Syndrome
|
|
|
| Heart Conduction Disease |
|
Conduction Disorder Of The Heart
|
Heart Rhythm Disease
|
|
|
| Cardiomyopathy, Familial Hypertrophic, 1 |
|
Asymmetric Septal Hypertrophy
|
Familial Hypertrophic Cardiomyopathy
|
|
Hypertrophic Cardiomyopathy 1
|
CMH1
|
|
Hypertrophic Cardiomyopathy 19
|
CMH
|
|
Ventricular Hypertrophy, Hereditary
|
Ash
|
|
Hypertrophic Subaortic Stenosis, Idiopathic
|
Cardiomyopathy, Familial Hypertrophic
|
|
Cardiomyopathy, Hypertrophic, 1, Digenic
|
Cardiomyopathy, Familial Hypertrophic 1
|
|
Hcm
|
Hereditary Ventricular Hypertrophy
|
|
Idiopathic Hypertrophic Subaortic Stenosis
|
Hypertrophic Cardiomyopathy
|
|
Cardiomyopathy, Hypertrophic, Familial
|
Cardiomyopathy, Hypertrophic, 1
|
|
Familial Asymmetric Septal Hypertrophy
|
Heritable Hypertrophic Cardiomyopathy
|
|
Fhc
|
Cardiomyopathy, Hypertrophic, Familial, Type 1
|
|
|
| Restrictive Cardiomyopathy |
|
Familial Restrictive Cardiomyopathy
|
Cardiomyopathy, Restrictive
|
|
Cardiomyopathy, Constrictive
|
Primary Restrictive Cardiomyopathy
|
|
Rcm
|
Cardiomyopathy Restrictive
|
|
|
| Dilated Cardiomyopathy |
|
Familial Dilated Cardiomyopathy
|
Primary Dilated Cardiomyopathy
|
|
Idiopathic Dilated Cardiomyopathy
|
Congestive Cardiomyopathy
|
|
Idiopathic Dilation Cardiomyopathy
|
Primary Familial Dilated Cardiomyopathy
|
|
Cardiomyopathy, Dilated
|
DCM
|
|
Cardiomyopathy, Familial Dilated
|
Dilated Cardiomyopathy, Familial
|
|
Hypokinetic Dilated Cardiomyopathy, Familial
|
Familial Idiopathic Cardiomyopathy
|
|
Fdc
|
Cardiomyopathy, Familial Idiopathic
|
|
Idiopathic Cardiomegaly
|
Dilated Congestive Cardiomyopathy
|
|
Chronic Dilated Cardiomyopathy
|
Ccm - [Congestive Cardiomyopathy]
|
|
Cocm - [Congestive Cardiomyopathy]
|
Dcm - [Dilated Cardiomyopathy]
|
|
Dilated-Hypokinetic Cardiomyopathy
|
Congestive Idiopathic Cardiomyopathy
|
|
Primary Idiopathic Dilated Cardiomyopathy
|
|
|
