| Diseases |
Alias |
|
| Supravalvular Aortic Stenosis |
|
SVAS
|
Supravalvar Aortic Stenosis
|
|
Supravalvar Aortic Stenosis, Eisenberg Type
|
Aortic Supravalvular Stenosis
|
|
Aortic Stenosis, Supravalvular
|
Supra-Valvular Aortic Stenosis
|
|
Stenosis, Aortic Supravalvular
|
Stenosis, Supravalvular Aortic
|
|
Supravalvular Stenosis, Aortic
|
Aortic Stenosis Supravalvular
|
|
|
| Cutis Laxa, Autosomal Dominant 1 |
|
Cutis Laxa, Autosomal Dominant
|
Autosomal Dominant Cutis Laxa
|
|
ADCL1
|
Adcl
|
|
Autosomal Dominant Cutis Laxa 1
|
Cutis Laxa, Autosomal Dominant, 1
|
|
Cutis Laxa, Autosomal Dominant, Type 1
|
|
|
| Williams-Beuren Syndrome |
|
Williams Syndrome
|
WBS
|
|
Wms
|
Deletion 7q11.23
|
|
Monosomy 7q11.23
|
Chromosome 7q11.23 Deletion Syndrome, 1.5- To 1.8-Mb
|
|
Fanconi Schlesinger Syndrome
|
Beuren Syndrome
|
|
Elfin Facies Syndrome
|
Elfin Facies With Hypercalcemia
|
|
Hypercalcemia-Supravalvar Aortic Stenosis
|
Ws
|
|
|
| Hypertelorism |
|
Eyes Wide Apart
|
Eyes Widely Set
|
|
Hypertelorism Of Orbit
|
Ocular Hypertelorism
|
|
Orbital Separation Excessive
|
|
|
| Cutis Laxa |
|
Generalized Elastolysis
|
Loose Skin
|
|
Dermatolysis
|
Dermatomegaly
|
|
Cutis Laxa Syndrome
|
|
|
| Pulmonary Emphysema |
|
|
| Exfoliation Syndrome |
|
Pseudoexfoliation Glaucoma
|
Pseudoexfoliation Syndrome
|
|
Exfoliation Syndrome, Susceptibility To
|
XFS
|
|
Exfoliation Glaucoma
|
Xfg
|
|
Pseudoexfoliation Of The Lens
|
Pexg
|
|
Pexs
|
Exfoliative Syndrome
|
|
Glaucoma Capsulare
|
Pex
|
|
Pseudo-Exfoliation Syndrome
|
|
|
| Aortic Disease |
|
Aortic Diseases
|
Aortic Disorder
|
|
Disorder Of The Aorta
|
|
|
| Buschke-Ollendorff Syndrome |
|
BOS
|
Dermatoosteopoikilosis
|
|
Dermatofibrosis Lenticularis Disseminata With Osteopoikilosis
|
Osteopathia Condensans Disseminata
|
|
Dermatofibrosis Lenticularis Disseminata
|
Disseminated Dermatofibrosis With Osteopoikilosis
|
|
Dermatofibrosis, Disseminated, With Osteopoikilosis
|
Osteopoikilosis With Or Without Melorheostosis
|
|
Dermatofibrosis, Disseminated With Osteopoikilosis
|
Dermatofibrosis Disseminata Lenticularis
|
|
Isolated Osteopoikilosis
|
Osteopoikilosis, Isolated
|
|
|
| Vascular Disease |
|
Vascular Diseases
|
Aneurysm
|
|
Spinal Cord Ischemia
|
Vascular Anomaly
|
|
Spinal Cord Vascular Diseases
|
Vascular Tissue Disease
|
|
|
| Aortic Aneurysm |
|
Aortic Rupture
|
Thoracoabdominal Aortic Aneurysm, Ruptured
|
|
Ruptured Aortic Aneurysm
|
Aortic Aneurysms
|
|
Aortic Aneurysm Without Mention Of Rupture Nos
|
Ruptured Abdominal Aortic Aneurysm
|
|
Aortic Aneurysm, Ruptured
|
Ruptured Thoracic Aortic Aneurysm
|
|
|
| Pseudoxanthoma Elasticum |
|
PXE
|
Gronblad-Strandberg Syndrome
|
|
Pseudoxanthoma Elasticum, Modifier Of Severity Of
|
Gronblad-Strandberg-Touraine Syndrome
|
|
Gronblad Strandberg Syndrome
|
Groenblad-Strandberg Syndrome
|
|
Nevus Elasticus
|
Pxe - [Pseudoxanthoma Elasticum]
|
|
|
| Arteriosclerosis |
|
Arteriosclerotic Vascular Disease
|
|
|
| Aortic Dissection |
|
|
| Marfan Syndrome |
|
MFS
|
Mfs1
|
|
Marfan'S Syndrome
|
Marfan Syndrome Type 1
|
|
Marfan Syndrome, Type I
|
Mass Phenotype
|
|
Contractural Arachnodactyly
|
Mass Syndrome
|
|
Octd
|
Overlap Connective Tissue Disease
|
|
Marfanoid Hypermobility Syndrome
|
Marfan Disease
|
|
|
| Aortic Aneurysm, Familial Thoracic 1 |
|
Thoracic Aortic Aneurysm
|
Annuloaortic Ectasia
|
|
Familial Thoracic Aortic Aneurysm And Aortic Dissection
|
Familial Aortic Dissection
|
|
Familial Taad
|
Familial Thoracic Aortic Aneurysm
|
|
Congenital Aneurysm Of Ascending Aorta
|
Familial Aortic Aneurysm
|
|
Familial Thoracic Aortic Aneurysm And Dissection
|
Aortic Aneurysm, Thoracic
|
|
AAT1
|
Faa1
|
|
Aortic Dissection, Familial
|
Aortic Aneurysm, Familial Thoracic
|
|
Aneurysm, Thoracic Aortic
|
Faa
|
|
Ftaad
|
Taa
|
|
Taad
|
Cystic Medial Necrosis Of Aorta
|
|
Familial Non-Syndromic Thoracic Aortic Aneurysm And Aortic Dissection
|
Aortic Aneurysm Thoracic
|
|
Familial Aortic Aneurysms
|
Aneurysm, Aortic, Thoracic, Familial, Type 1
|
|
Aneurysm Of Thoracic Aorta
|
Intrathoracic Aneurysm
|
|
Thoracic Aorta Aneurysm
|
Thoracic Aortic Aneurysm Without Rupture
|
|
Thoracic Aneurysm
|
Thorax Arterial Aneurysm
|
|
Thoracic Artery Aneurysm
|
Thoracic Arterial Aneurysm
|
|
Thorax Aneurysm
|
Thorax Aortic Aneurysm
|
|
Dissection Of Thoracic Aorta
|
|
|
| Ehlers-Danlos Syndrome, Vascular Type |
|
Eds Iv
|
Eds4
|
|
Vascular Ehlers-Danlos Syndrome
|
Veds
|
|
Sack-Barabas Syndrome
|
EDSVASC
|
|
Ehlers-Danlos Syndrome, Type Iv, Autosomal Dominant
|
Vascular Type Ehlers-Danlos Syndrome
|
|
Arterial-Ecchymotic Eds
|
Ehlers-Danlos Syndrome Type 4
|
|
Vascular Eds
|
Ehlers-Danlos Syndrome, Type 4
|
|
Ehlers-Danlos Syndrome, Type Iv
|
Ehlers-Danlos Syndrome, Arterial Type
|
|
Ehlers-Danlos Syndrome, Ecchymotic Type
|
Ehlers-Danlos Syndrome, Sack-Barabas Type
|
|
Autosomal Dominant Type Iv Ehlers-Danlos Syndrome
|
Eds Type Iv
|
|
Eds Type 4
|
Ehlers Danlos Syndrome, Sack-Barabas Type
|
|
Ehlers Danlos Syndrome, Arterial Type
|
Ehlers Danlos Syndrome, Ecchymotic Type
|
|
Ehlers-Danlos Syndrome Type Iv
|
Ehlers-Danlos Syndrome 4
|
|
Ehlers-Danlos Syndrome Arterial Type
|
Ehlers-Danlos Syndrome Ecchymotic Type
|
|
Ehlers-Danlos Syndrome, Type 4 Variant
|
Ehlers-Danlos, Vascular Type Syndrome
|
|
|
| Aortic Aneurysm, Familial Abdominal, 1 |
|
Abdominal Aortic Aneurysm
|
Aortic Aneurysm, Familial Abdominal 1
|
|
Aneurysm, Abdominal Aortic
|
AAA
|
|
Aortic Aneurysm, Abdominal
|
AAA1
|
|
Aortic Aneurysm, Familial Abdominal
|
Aortic Aneurysm Abdominal
|
|
Abdominal Aortic Aneurysms
|
Abdominal Aortic Aneurysm Without Mention Of Perforation Or Rupture
|
|
Abdomen Aneurysm
|
Abdominal Aorta Aneurysm
|
|
Aneurysm Of Abdominal Aorta
|
Aortic Abdomen Aneurysm
|
|
Aaa - [Abdominal Aortic Aneurysm]
|
Abdominal Aneurysm
|
|
Abdominal Aorta Aneurysm Rupture
|
Abdominal Aorta Aneurysm Ruptured
|
|
Abdominal Aortic Aneurysm Which Has Ruptured
|
Ruptured Aaa
|
|
Abdomen Aorta Aneurysm Ruptured
|
Abdomen Aorta Rupture
|
|
Abdomen Aortic Aneurysm Rupture
|
Abdomen Aneurysm Rupture
|
|
Abdomen Aortic Aneurysm Ruptured
|
Abdomen Aortic Rupture
|
|
Abdominal Aorta Rupture
|
Abdominal Aortic Rupture
|
|
Rupture Abdomen Aorta Aneurysm
|
Rupture Abdominal Aortic Aneurysm
|
|
Ruptured Abdomen Aneurysm
|
Ruptured Abdomen Aorta
|
|
Ruptured Abdomen Aortic
|
Ruptured Abdominal Aneurysm
|
|
Ruptured Abdominal Aorta
|
Ruptured Abdominal Aortic
|
|
Ruptured Aorta Abdominalis Aneurysm
|
False Abdomen Aorta Aneurysm Ruptured
|
|
False Abdominal Aortic Aneurysm Ruptured
|
False Abdominal Aorta Aneurysm Ruptured
|
|
False Abdomen Aortic Aneurysm Ruptured
|
|
|
| Osteopoikilosis |
|
Osteopathia Condensans Disseminata
|
Spotted Bones
|
|
Dermatofibrosis Lenticularis Disseminata
|
|
|
| Aortic Valve Disease 2 |
|
Aortic Valve Stenosis
|
Aortic Stenosis
|
|
Rheumatic Aortic Stenosis
|
AOVD2
|
|
Bicuspid Aortic Valve
|
Rheumatic Aortic Valve Stenosis
|
|
Valvular Aortic Stenosis
|
Aortic Valve Disease, Type 2
|
|
Aortic Valve Stricture
|
Aortic Valve Obstruction
|
|
Obstructed Aorta Valve
|
Rheumatic Aortic Obstruction
|
|
Rheumatic Aortic Valve Obstruction
|
Rheumatic Aortic Stricture
|
|
Aortic Valve Regurgitation
|
Aortic Insufficiency With Stenosis
|
|
Rheumatic Aortic Valve Stenosis With Insufficiency
|
Rheumatic Aortic Stenosis With Incompetence
|
|
Rheumatic Aortic Stenosis With Regurgitation
|
|
|
| Menkes Disease |
|
Copper Transport Disease
|
Menkes Syndrome
|
|
MNK
|
Kinky Hair Disease
|
|
Steely Hair Disease
|
Menkes Kinky-Hair Syndrome
|
|
Mk
|
Steely Hair Syndrome
|
|
Menkea Syndrome
|
Md
|
|
Menkes Kinky Hair Syndrome
|
Hypocupremia, Congenital
|
|
Kinky Hair Syndrome
|
X-Linked Copper Deficiency
|
|
Menkes Kinky Hair Disease
|
|
|
| Pelvic Organ Prolapse |
|
Rectal Prolapse
|
Pelvic Organ Prolapse, Susceptibility To, 1
|
|
Pelvic Organ Prolapse, Susceptibility To
|
Prolapse Of Vagina And Rectum
|
|
Vaginal Prolapse
|
Pelvic Organ Prolapse 1
|
|
Procidentia, Rectum
|
Prolapse Of Rectal Mucosa
|
|
Procidentia Of Rectum
|
Rectal Mucosa Prolapse
|
|
Rectum Prolapse
|
Procidentia Rectum
|
|
Rp - [Rectal Prolapse]
|
Male Proctocele
|
|
Male Rectocele
|
Proctoptosis
|
|
Female Genital Prolapse
|
Female Prolapse
|
|
Incompetence Of Pelvic Fundus
|
Relaxation Of Perineum
|
|
Deficiency Of Perineum
|
|
|
| Alpha-1-Antitrypsin Deficiency |
|
Alpha 1-Antitrypsin Deficiency
|
Alpha-1 Antitrypsin Deficiency
|
|
Aat Deficiency
|
Aatd
|
|
A1ATD
|
Emphysema Due To Aat Deficiency
|
|
A1at Deficiency
|
Emphysema-Cirrhosis, Due To Aat Deficiency
|
|
Hemorrhagic Diathesis Due To Antithrombin Pittsburgh
|
Alpha-1 Antiprotease Deficiency
|
|
Alpha 1 Antitrypsin Deficiency
|
Aat
|
|
Alpha-1 Protease Inhibitor Deficiency
|
Alpha-1 Related Emphysema
|
|
Genetic Emphysema
|
Hereditary Pulmonary Emphysema
|
|
Inherited Emphysema
|
Alpha-1-Proteinase Inhibitor Deficiency
|
|
Alpha1-Antitrypsin Deficiency
|
Alpha-1-Antitrypsin Deficiency, Autosomal Recessive
|
|
Emphysema, Hereditary Pulmonary
|
Aatd - [Alpha-1-Antitrypsin] Deficiency
|
|
|
| Elephantiasis |
|
|
| Aortic Valve Disease 1 |
|
Aortic Valve Disease
|
Bicuspid Aortic Valve
|
|
Aortic Valve Disorder
|
AOVD1
|
|
Bav
|
Bicuspid Aortic Valve Disease
|
|
Familial Bicuspid Aortic Valve
|
Aortic Valve Calcification
|
|
Aovd
|
Aortic Valve, Bicuspid
|
|
Aortic Valve, Calcification Of
|
Aortic Stenosis, Calcific
|
|
Familial Bav
|
Calcific Aortic Stenosis
|
|
Calcification Of Aortic Valve
|
Abnormality Of The Aortic Valve
|
|
Aortic Valve Disease, Type 1
|
Aortic Valve Disease 2
|
|
Bicommissural Aortic Valve
|
|
|
| Adult Respiratory Distress Syndrome |
|
Acute Respiratory Distress Syndrome
|
Ards
|
|
Non-Cardiogenic Pulmonary Edema
|
Acute Lung Injury
|
|
Respiratory Distress Syndrome, Adult
|
Shock Lung
|
|
Acute Respiratory Distress
|
Respiratory Distress Syndrome
|
|
Adult Rds
|
Ali
|
|
Increased-Permeability Pulmonary Edema
|
Stiff Lung
|
|
Respiratory Distress Syndrome Adult
|
|
|
| Open-Angle Glaucoma |
|
Glaucoma Simplex
|
Pigmentary Glaucoma
|
|
Wide-Angle Glaucoma
|
Glaucoma, Open-Angle
|
|
Open Angle Glaucoma
|
Glaucoma Open-Angle
|
|
Chronic Simple Glaucoma
|
Coag - [Chronic Open-Angle Glaucoma]
|
|
Csg - [Chronic Simple Glaucoma]
|
Poag - [Primary Open-Angle Glaucoma]
|
|
Oag - [Open-Angle Glaucoma]
|
Chronic Glaucoma
|
|
Chronic Open Angle Glaucoma
|
Simple Glaucoma
|
|
Chronic Noncongestive Glaucoma
|
Ltg - [Low Tension Glaucoma]
|
|
Noncongestive Glaucoma
|
Nonobstructive Glaucoma
|
|
Normal Pressure Glaucoma
|
Primary Low Tension Glaucoma
|
|
Low-Tension Glaucoma
|
Residual Stage Low Tension Glaucoma
|
|
Open Cleft Glaucoma
|
|
|
| Pneumothorax |
|
Pneumothorax Nos
|
Air Leak Nos
|
|
Pleural Air Leak Nos
|
|
|
| Elastosis Perforans Serpiginosa |
|
EPS
|
Elastoma Intrapapillare Perforans Verruciformis
|
|
Miescher Elastoma
|
|
|
| Costello Syndrome |
|
Faciocutaneoskeletal Syndrome
|
Fcs Syndrome
|
|
Congenital Myopathy With Excess Of Muscle Spindles
|
CSTLO
|
|
CMEMS
|
Fcss
|
|
Myopathy, Congenital, With Excess Of Muscle Spindles
|
|
|
| Collagen Disease |
|
Collagen Diseases
|
Collagen Disorder
|
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Varicose Veins |
|
Varices
|
Varix
|
|
Venous Ectasia
|
Venous Varices
|
|
Varicosity
|
|
|
| Gm1 Gangliosidosis |
|
Beta-Galactosidase Deficiency
|
Gangliosidosis Gm1
|
|
Deficiency Of Beta-Galactosidase
|
Beta Galactosidase 1 Deficiency
|
|
Beta-Galactosidosis
|
Glb 1 Deficiency
|
|
Beta-Galactosidase-1 Deficiency
|
Beta-Galactosidase-1 Deficiency
|
|
Glb1 Deficiency
|
Landing Disease
|
|
Gangliosidosis, Gm1
|
|
|
| Phimosis |
|
Tight Foreskin
|
Tight Frenulum
|
|
Congenital Phimosis
|
|
|
| Gangliosidosis |
|
|
| Glaucoma, Primary Open Angle |
|
Glaucoma 1, Open Angle, E
|
Primary Open Angle Glaucoma
|
|
POAG
|
Adult-Onset Primary Open Angle Glaucoma
|
|
Chronic Simple Glaucoma
|
GLC1E
|
|
Primary Open Angle Glaucoma 1e
|
Glaucoma, Open Angle, Primary
|
|
|
| Lung Disease |
|
Lung Diseases
|
Disorder Of Lung
|
|
Abnormality Of The Lung
|
|
|
| Idiopathic Scoliosis |
|
|
| Cerebral Aneurysms |
|
Cerebral Aneurysm
|
Cerebral Arterial Aneurysm
|
|
|
| Pulmonary Fibrosis |
|
|
| Lymphangioleiomyomatosis |
|
Lymphangiomyomatosis
|
LAM
|
|
Lung Lymphangioleiomyomatosis
|
Pulmonary Lymphangioleiomyomatosis
|
|
Lymphangioleiomyomatosis, Somatic
|
Lymphangio-Myomatosis
|
|
|
| Perineocele |
|
|
| Pulmonary Disease, Chronic Obstructive |
|
Chronic Obstructive Pulmonary Disease
|
COPD
|
|
Pulmonary Disease, Chronic Obstructive, Severe Early-Onset
|
Chronic Obstructive Lung Disease
|
|
Chronic Obstructive Airway Disease
|
Pulmonary Disease, Chronic Obstructive, Susceptibility To
|
|
Cold
|
Severe Early-Onset Chronic Obstructive Pulmonary Disease
|
|
Pulmonary Disease Chronic Obstructive
|
Pulmonary Disease, Obstructive, Chronic, Susceptibility To
|
|
Chronic Obstructive Pulmonary Disease Of Horses
|
Common Cold
|
|
Upper Respiratory Infections
|
Copd - [Chronic Obstructive Pulmonary Disease]
|
|
Coad - [Chronic Obstructive Airways Disease]
|
Cold - [Chronic Obstructive Lung Disease]
|
|
Chronic Airway Disease Nos
|
Chronic Airways Limitation, Unspecified
|
|
Chronic Obstructed Airway, Unspecified
|
Chronic Obstructive Airway Disease, Unspecified
|
|
Chronic Obstructive Airway, Unspecified
|
Obstructive Lung Disease Nos
|
|
Chronic Obstructive Lung Disease Nos
|
Chronic Obstructive Lung Nos
|
|
Obstructive Pulmonary Disease Nos
|
Exacerbation Copd Nos
|
|
Acute Exacerbation Copd
|
|
|
| Phacogenic Glaucoma |
|
|
| Rheumatic Heart Disease |
|
Rheumatic Carditis
|
Rheumatic Congestive Heart Failure
|
|
Congestive Rheumatic Heart Failure
|
Rheumatic Heart Failure
|
|
RHD
|
Rheumatic Fever Inactive Or Quiescent With Heart Disease
|
|
Rheumatic Fever Inactive Or Quiescent With Carditis
|
Organ Rheumatic Heart Disease
|
|
Organic Rheumatic Heart Disease
|
Inactive Rheumatic Heart Disease
|
|
Rheumatic Heart
|
Rheumatic Fever Inactive Or Quiescent With Pancarditis
|
|
Rhd - [Rheumatic Heart Disease]
|
Rheumatic Cardiac Hypertrophy
|
|
Rheumatic Fever
|
Inactive Or Quiescent With Cardiac Hypertrophy
|
|
Rheumatic Pancarditis
|
Inactive Rhd - [Rheumatic Heart Disease]
|
|
Rheumatic Nonischaemic Cardiopathy
|
|
|
| Oral Submucous Fibrosis |
|
Oral Submucosal Fibrosis, Including Of Tongue
|
Osmf
|
|
Oral Cavity Submucous Fibrosis
|
Oral Submucosal Fibrosis
|
|
Submucosal Fibrosis
|
|
|
| Aortic Valve Insufficiency |
|
Aortic Regurgitation
|
Rheumatic Aortic Regurgitation
|
|
Aortic Insufficiency
|
Rheumatic Aortic Insufficiency
|
|
Rheumatic Aortic Valve Insufficiency
|
Aortic Incompetence
|
|
Corrigan'S Disease
|
Rheumatic Aortic Valve Regurgitation
|
|
Aortic Valve Incompetency
|
Ai - [Aortic Incompetence]
|
|
Incompetent Aortic Valve
|
Ar - [Aortic Regurgitation]
|
|
Calcific Aortic Valve Regurgitation
|
Myxomatous Aortic Valve Regurgitation
|
|
Annular Incompetency Of Aortic Valve
|
Austin Flint Murmur
|
|
Flint Murmur
|
Rheumatic Aortic Incompetence
|
|
Rheumatic Ai - [Aortic Insufficiency]
|
|
|
| Intraocular Pressure Quantitative Trait Locus |
|
Glaucoma
|
IOPQTL
|
|
Glaucoma, Susceptibility To
|
Postinfectious Glaucoma
|
|
Glaucoma With Ocular Inflammation
|
Glaucoma Secondary To Eye Inflammation
|
|
Traumatic Glaucoma
|
Glaucoma With Concussion Of Globe
|
|
Glaucoma Due To Ocular Trauma
|
Glaucoma Associated With Ocular Trauma
|
|
Glaucoma Secondary To Drugs
|
|
|
| Erysipelas |
|
|
| Autosomal Recessive Cutis Laxa Type I |
|
Autosomal Recessive Cutis Laxa Type 1
|
Cutis Laxa, Type 1
|
|
Cutis Laxa, Autosomal Recessive, Type I
|
Cutis Laxa, Autosomal Recessive Type 1
|
|
Cutis Laxa, Autosomal Recessive
|
Arcl1
|
|
Autosomal Recessive Cutis Laxa With Severe Systemic Involvement
|
Autosomal Recessive Cutis Laxa, Pulmonary Emphysema Type
|
|
|
| Cutis Laxa, Autosomal Recessive, Type Ia |
|
ARCL1A
|
Cutis Laxa, Autosomal Recessive
|
|
Autosomal Recessive Cutis Laxa Type Ia
|
Cutis Laxa, Autosomal Recessive, Type 1a
|
|
Arcl1
|
Cutis Laxa, Autosomal Recessive, 1a
|
|
Cl Type I
|
Cutis Laxa Autosomal Recessive Type I
|
|
Cutis Laxa Autosomal Recessive Type Ia
|
Cutis Laxa, Autosomal Recessive, Type I
|
|
|
| Bronchiectasis |
|
Polynesian Bronchiectasis
|
Kartagener Syndrome
|
|
Bronchiectasis Nos
|
|
|
| Telangiectasis |
|
|
| Arterial Tortuosity Syndrome |
|
Arterial Tortuosity
|
Ats
|
|
ATORS
|
Tortuosity, Arterial, Syndrome
|
|
|
| Connective Tissue Disease |
|
Connective Tissue Diseases
|
Connective Tissue Disorder
|
|
Abnormality Of Connective Tissue
|
Disorder Of Connective Tissue
|
|
Connective Tissue Disorders
|
|
|
| Heart Disease |
|
Heart Failure
|
Congenital Heart Disease
|
|
Heart Diseases
|
Congenital Heart Defects
|
|
Congenital Heart Defect
|
Heart Malformation
|
|
Congenital Anomaly Of Heart
|
Heart Defect
|
|
Heart-Congenital Defect
|
Congenital Heart Disorder
|
|
Heart Defects Congenital
|
Heart Defects, Congenital
|
|
Heart Defects
|
Heart Disease, Congenital
|
|
Disease, Heart, Congenital
|
Congestive Heart Failure
|
|
|
| Bladder Diverticulum |
|
Diverticulum Of Bladder
|
Diverticulum - Bladder
|
|
Bladder Diverticula
|
Vesical Diverticulum
|
|
Bladder Sacculation
|
|
|
| Aortitis |
|
|
| Kawasaki Disease |
|
Mucocutaneous Lymph Node Syndrome
|
Acute Febrile Mucocutaneous Lymph Node Syndrome
|
|
Kawasaki Syndrome
|
Kd
|
|
Infantile Polyarteritis
|
Kawasaki Disease, Susceptibility To
|
|
Acute Febrile Mcls
|
Kawasaki'S Disease
|
|
Mlns
|
KWD
|
|
|
| Atherosclerosis Susceptibility |
|
Atherosclerosis
|
Atherosclerosis, Susceptibility To
|
|
ATHS
|
Atherogenic Lipoprotein Phenotype
|
|
Alp
|
Arteriosclerosis
|
|
|
| Angioid Streaks |
|
|
| Retinal Detachment |
|
Retinal Detachments
|
Rhegmatogenous Retinal Detachment
|
|
Ruptured Retina With Detachment
|
Retinal Hole With Detachment
|
|
|
| Peyronie'S Disease |
|
Induratio Penis Plastica
|
Peyronie Disease
|
|
Peyronies Disease
|
Peyronie'S Fibromatosis
|
|
Penile Induration
|
Balanitis Xerotica Obliterans
|
|
|
| Optic Nerve Disease |
|
Optic Neuropathy
|
Disorder Of The Second Nerve
|
|
Optic Nerve Disorder
|
Optic Nerve
|
|
Abnormality Of The Optic Nerve
|
Optic Nerve Disorders
|
|
Neuropathy, Optic
|
Disorder Of The Optic Nerve
|
|
|
| Subclavian Artery Aneurysm |
|
Aneurysm Of Subclavian Artery
|
|
|
| Diaphragmatic Hernia, Congenital |
|
Congenital Diaphragmatic Hernia
|
Diaphragmatic Hernia
|
|
Cdh
|
Congenital Diaphragmatic Defect
|
|
Hernia, Diaphragmatic
|
Dih
|
|
Hernia, Congenital Diaphragmatic
|
Hcd
|
|
Diaphragmatic Defect, Congenital
|
Diaphragm, Unilateral Agenesis Of
|
|
Hemidiaphragm, Agenesis Of
|
Diaphragmatic Hernia 1
|
|
Agenesis Of Hemidiaphragm
|
Unilateral Agenesis Of Diaphragm
|
|
Hernia Diaphragmatic
|
Hernia Diaphragmatic Congenital
|
|
Hernia, Diaphragmatic, Type 1
|
Hiatus Hernia
|
|
Oesophageal Hiatus Hernia
|
Paraoesophageal Hernia
|
|
Sliding Hiatus Hernia
|
Congenital Diaphragm Hernia
|
|
Congenital Diaphragm Defect With Hernia
|
Gross Congenital Diaphragm Defect
|
|
|
| Contractural Arachnodactyly, Congenital |
|
Congenital Contractural Arachnodactyly
|
Beals Syndrome
|
|
CCA
|
Beals-Hecht Syndrome
|
|
Distal Arthrogryposis Type 9
|
Arthrogryposis, Distal, Type 9
|
|
Da9
|
Arachnodactyly, Contractural Beals Type
|
|
Contractures, Multiple With Arachnodactyly
|
Ear Anomalies-Contractures-Dysplasia Of Bone With Kyphoscoliosis
|
|
Arthrogyroposis, Distal, Type 9
|
Distal Arthrogyropsis Type 9
|
|
Cca Syndrome
|
Arachnodactyly
|
|
|
| Intravascular Fasciitis |
|
Intravascular Pseudosarcomatous Fasciitis
|
|
|
| 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
|
|
|
| Heart Valve Disease |
|
Heart Valve Diseases
|
Valvular Heart Disease
|
|
Valvular Heart Diseases
|
Heart Valve Prolapse
|
|
|
| Loeys-Dietz Syndrome |
|
Loeys-Dietz Aortic Aneurysm Syndrome
|
Lds
|
|
Aortic Aneurysm Syndrome Due To Tgf-Beta Receptors Anomalies
|
Furlong Syndrome
|
|
|
| Cystic Fibrosis |
|
Mucoviscidosis
|
CF
|
|
Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis
|
Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis
|
|
Cystic Fibrosis Lung Disease, Modifier Of
|
Cystic Fibrosis Of Pancreas
|
|
Fibrocystic Disease Of Pancreas
|
Cf - [Cystic Fibrosis]
|
|
Cystic Fibrosis Nos
|
Fibrocystic Disease
|
|
Fibrocystic Disease Of The Pancreas
|
Mucoviscidosis Of Pancreas
|
|
Nonproliferative Fibrocystic Disease
|
Pancreatic Cystic Fibrosis
|
|
|
| Stiff Skin Syndrome |
|
|
| Steroid-Induced Glaucoma |
|
Corticosteroid-Induced Glaucoma
|
|
|
| Occipital Horn Syndrome |
|
OHS
|
Eds Ix
|
|
Cutis Laxa X-Linked
|
Cutis Laxa, X-Linked
|
|
Cutis Laxa, X-Linked, Formerly
|
Ehlers-Danlos Syndrome, Occipital Horn Type, Formerly
|
|
Eds Ix, Formerly
|
Eds9, Formerly
|
|
Ehlers-Danlos Syndrome Type 9
|
Ehlers-Danlos Syndrome Type Ix
|
|
X-Linked Cutis Laxa
|
Ehlers-Danlos Syndrome, Occipital Horn Type
|
|
Eds9
|
Ehlers-Danlos Syndrome Occipital Horn Type
|
|
|
| Necrobiosis Lipoidica |
|
Oppenheim-Urbach Disease
|
Necrobiosis Lipoidica Diabeticorum
|
|
|
| Plasma Protein Metabolism Disease |
|
|
| Keratoconus |
|
Kc
|
Conical Cornea
|
|
Noninflammatory Corneal Thining
|
Bulging Cornea
|
|
Cornea Conical
|
Acquired Conus Of Cornea
|
|
|
| Cutis Laxa, Autosomal Recessive, Type Ib |
|
ARCL1B
|
Cutis Laxa, Autosomal Recessive, Type 1b
|
|
Autosomal Recessive Cutis Laxa Type Ib
|
Lethal Arteriopathy Syndrome Due To Fibulin-4 Deficiency
|
|
Cutis Laxa, Autosomal Recessive, 1b
|
Cutis Laxa Autosomal Recessive Type Ib
|
|
|
| Scoliosis |
|
|
| Homocysteinemia |
|
|
| Orthostatic Intolerance |
|
Mitral Valve Prolapse
|
Neurocirculatory Asthenia
|
|
Mitral Valve Prolapse Syndrome
|
Irritable Heart
|
|
Systolic Click-Murmur Syndrome
|
Soldiers Heart
|
|
Cardiovascular Malfunction Arising From Mental Factors
|
Cardiovascular Neurosis
|
|
Da Costa'S Syndrome
|
Krishaber'S Disease
|
|
Barlow'S Syndrome
|
Floppy Mitral Valve
|
|
Mitral Leaflet Syndrome
|
Myxomatous Mitral Valve Prolapse
|
|
Postural Orthostatic Tachycardia Syndrome Due To Net Deficiency
|
Familial Orthostatic Tachycardia Due To Norepinephrine Transporter Deficiency
|
|
Orthostatic Intolerance Due To Net Deficiency
|
Pots Due To Net Deficiency
|
|
OI
|
Intolerance, Orthostatic
|
|
Mitral Valve Prolapse, Familial, X-Linked
|
Ballooning Mitral Valve
|
|
Barlow Syndrome
|
Flail Mitral Leaflet
|
|
Myxomatous Mitral Valve
|
Mitral Valve Prolapse-Click Syndrome
|
|
Prolapsing Mitral Valve Leaflet Syndrome
|
Billowing Mitral Valve Leaflet
|
|
Posterior Mitral Leaflet Deformity
|
Ballooning Posterior Leaflet Syndrome
|
|
Blue Valve Syndrome
|
Floppy Mitral Valve Syndrome
|
|
Mitral Valvular Prolapse
|
Systolic Click Syndrome
|
|
|
| Cerebral Arterial Disease |
|
Cerebral Arterial Diseases
|
|
|
| Inguinal Hernia |
|
Hernia Inguinal
|
Hernia, Inguinal
|
|
Inguinal Hernias
|
Bubonocele
|
|
Indirect Inguinal Hernia
|
Direct Inguinal Hernia
|
|
Oblique Inguinal Hernia
|
Scrotal Hernia
|
|
Ih - [Inguinal Hernia]
|
|
|
| Hutchinson-Gilford Progeria Syndrome |
|
Progeria
|
HGPS
|
|
Hutchinson-Gilford Syndrome
|
Hutchinson-Gilford Progeria
|
|
Hutchinson Gilford Syndrome
|
Hutchinson Gilford Progeria Syndrome
|
|
Hutchinson-Gilford Disease
|
Progeria Of Childhood
|
|
Hutchinson-Gilford-Progeria Syndrome
|
|
|
| Palmoplantar Keratoderma, Punctate Type Iii |
|
Acrokeratoelastoidosis Of Costa
|
Ake
|
|
Punctate Palmoplantar Keratoderma Type Iii
|
PPKP3
|
|
Keratoderma, Palmoplantar, Punctate Type 3
|
Punctate Palmoplantar Hyperkeratosis Type 3
|
|
Punctate Palmoplantar Keratoderma Type 3
|
Rare Form Of Hirschsprung'S Disease
|
|
Acrokeratoelastoidosis
|
Collagenous Plaques Of Hands And Feet
|
|
Aganglionosis, Total Intestinal
|
Collagenous Plaques Of Hand And Feet
|
|
Palmoplantar Keratoderma, Punctate Type 3
|
Aganglionosis, Total Colonic
|
|
Ntia
|
Near-Total Intestinal Aganglionosis
|
|
Tia
|
|
|
| Iris Disease |
|
|
| Wrinkly Skin Syndrome |
|
WSS
|
Wrinkled Skin Syndrome
|
|
|
| Pulmonary Hypertension |
|
Primary Pulmonary Hypertension
|
Hypertension Pulmonary
|
|
Hypertension, Pulmonary
|
Hypertension, Pulmonary, Primary
|
|
Idiopathic Pulmonary Hypertension
|
Idiopathic Pulmonary Arterial Hypertension
|
|
Pulmonary Htn - [Hypertension]
|
|
|
| Lichen Sclerosus Et Atrophicus |
|
Lichen Sclerosus
|
LSA
|
|
Lichen Sclerosis
|
Lichen Sclerosis Et Atrophicus
|
|
Ls Et A - [Lichen Sclerosus Et Atrophicus]
|
Lichen Albus
|
|
|
| Autosomal Recessive Cutis Laxa Type Ii Classic Type |
|
Arcl2, Classic Type
|
Arcl2, Debre Type
|
|
Autosomal Recessive Cutis Laxa Type 2, Classic Type
|
Autosomal Recessive Cutis Laxa Type 2, Debre Type
|
|
|
| Chronic Venous Insufficiency |
|
|
| Papillary Squamous Carcinoma |
|
Papillary Epidermoid Carcinoma
|
Papillary Squamous Cell Carcinoma
|
|
|
| Tracheal Stenosis |
|
|
| Cardiovascular System Disease |
|
Abnormality Of The Cardiovascular System
|
Cardiovascular Disease
|
|
Disease Of Subdivision Of Hemolymphoid System
|
Disorder Of Cardiovascular System
|
|
Cardiovascular Diseases
|
|
|
| Loeys-Dietz Syndrome 4 |
|
LDS4
|
Aneurysm, Aortic And Cerebral, With Arterial Tortuosity And Skeletal Manifestations
|
|
Loeys-Dietz Syndrome Type 4
|
Aortic And Cerebral Aneurysm With Arterial Tortuosity And Skeletal Manifestations
|
|
Loeys-Dietz Syndrome, Type 4
|
|
|
| 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
|
|
|
| Decubitus Ulcer |
|
Pressure Ulcer
|
Pressure Sores
|
|
Pressure Ulcers
|
Bedsore
|
|
Decubitus Ulcer
|
Decubitus Ulcer Any Site
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Endocardial Fibroelastosis |
|
Endomyocardial Fibroelastosis
|
Elastomyofibrosis
|
|
EFE
|
Efe - [Endocardial Fibroelastosis]
|
|
Primary Endocardial Fibroelastosis
|
Fibroelastosis Cordis
|
|
Fetal Endocarditis
|
Fibroelastosis
|
|
Congenital Endocardial Fibroelastosis
|
Congenital Valvular Endocarditis
|
|
|
| Granulomatosis With Polyangiitis |
|
GPA
|
Wegener Granulomatosis
|
|
Wegener Granulomatosis, Formerly
|
Midline Granulomatosis
|
|
Wg, Formerly
|
Necrotizing Respiratory Granulomatosis
|
|
Wg
|
Wegeners Granulomatosis
|
|
Pauci-Immune Glomerulonephritis Associated With Granulomatosis With Polyangiitis
|
|
|
| Lymphoid Interstitial Pneumonia |
|
Lymphocytic Interstitial Pneumonia
|
Lip Disease
|
|
Lip Diseases
|
LIP
|
|
Disease Of Lips
|
|
|
| Microcephaly And Chorioretinopathy 1 |
|
|
| Chromosomal Deletion Syndrome |
|
|
| Moyamoya Disease 1 |
|
Moyamoya Disease
|
Spontaneous Occlusion Of The Circle Of Willis
|
|
Mymy
|
Progressive Intracranial Arterial Occlusion
|
|
Moyamoya Syndrome
|
MYMY1
|
|
Cerebrovascular Moyamoya Disease
|
Moya-Moya Disease
|
|
Progressive Intracranial Occlusive Arteropathy
|
Idiopathic Moyamoya Disease
|
|
|
| Polycystic Kidney Disease 4 |
|
|
| Patent Ductus Arteriosus 1 |
|
Patent Ductus Arteriosus
|
PDA1
|
|
Pda
|
Ductus Arteriosus, Patent
|
|
Patent Ductus Arteriosus, Susceptibility To
|
Patent Ductus Botalli
|
|
Patency Of The Ductus Arteriosus
|
Patent Ductus Arteriosus Familial
|
|
Ductus Arteriosus Patent
|
Patent Ductus Arteriosus - Persisting Type
|
|
|
| Weill-Marchesani Syndrome |
|
Gemss Syndrome
|
Spherophakia-Brachymorphia Syndrome
|
|
Marchesani-Weill Syndrome
|
Wms
|
|
Congenital Mesodermal Dystrophy
|
Mesodermal Dysmorphodystrophy, Congenital
|
|
Spherophakia Brachymorphia Syndrome
|
Mesodermal Dysmorphodystrophy Congenital
|
|
Wm Syndrome
|
Brachydactyly-Spherophakia Syndrome
|
|
Brachymorphy With Spherophakia Syndrome
|
Congenital Mesodermal Dysmorphodystrophy
|
|
Marchesani Syndrome
|
Weill-Marchesani Syndrome, Autosomal Recessive
|
|
Weill-Marchesani Syndrome, Autosomal Dominant
|
|
|
| Ureteric Orifice Cancer |
|
Malignant Neoplasm Of Ureteric Orifice Of Urinary Bladder
|
Malignant Tumor Of Ureteric Orifice
|
|
Orifice Of The Ureter
|
|
|
| Macular Degeneration, Age-Related, 1 |
|
Macular Degeneration
|
Age-Related Macular Degeneration
|
|
Macular Degeneration, Age-Related
|
Age Related Macular Degeneration
|
|
Age Related Macular Degeneration 1
|
ARMD1
|
|
Senile Macular Degeneration
|
Maculopathy, Age-Related, 1
|
|
Macular Degeneration, Age-Related, Reduced Risk Of
|
Age Related Maculopathy 1
|
|
Age Related Maculopathies
|
Age Related Maculopathy
|
|
Senile Macular Retinal Degeneration
|
Macular Degeneration Of Retina
|
|
Age-Related Maculopathy
|
Amd
|
|
Armd
|
Age-Related Maculopathy, Susceptibility To
|
|
Maculopathy Age-Related
|
Macular Degeneration, Age-Related, 1, Susceptibility To
|
|
Maculopathy, Age-Related
|
Macular Degeneration, Age-Related, Type 1
|
|
Macular Degeneration, Age-Related, 2
|
|
|
| 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]
|
|
|
| Osteogenesis Imperfecta, Type Xi |
|
Osteogenesis Imperfecta Type 11
|
OI11
|
|
Osteogenesis Imperfecta Type Xi
|
Oi, Type Xi
|
|
Osteogenesis Imperfecta 11
|
Oi Type Xi
|
|
Oi-Xi
|
|
|
| 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
|
|
|
| Stickler Syndrome |
|
Arthroophthalmopathy
|
Hereditary Arthro-Ophthalmo-Dystrophy
|
|
Hereditary Arthro-Ophthalmopathy
|
Stickler Dysplasia
|
|
Hereditary Progressive Arthroophthalmopathy
|
Stickler Syndrome, Type 1
|
|
|
| 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
|
|
|
| Skin Disease |
|
Skin Diseases
|
Genodermatosis
|
|
Abnormality Of The Skin
|
Skin Diseases, Genetic
|
|
Skin And Subcutaneous Tissue Disease
|
Dermatologic Disorders
|
|
|
| Muscular Dystrophy |
|
Muscular Dystrophies
|
Congenital Md
|
|
Congenital Muscular Dystrophy
|
Cmd
|
|
Mdc
|
Dystrophy, Muscular
|
|
Gower'S Muscular Dystrophy
|
Progressive Musclular Dystrophy
|
|
Pseudohypertrophic Atrophy
|
Pseudohypertrophic Muscle Paralysis
|
|
Pseudohypertrophic Muscular Atrophy
|
Pseudohypertrophic Muscular Dystrophy
|
|
Pseudohypertrophic Paralysis
|
Pseudomuscular Hypertrophy
|
|
|
| Hypoplastic Left Heart Syndrome |
|
Hlhs
|
Heart, Hypoplastic Left, Syndrome
|
|
Hypoplasia Of The Left Heart
|
Left Heart Hypoplasia Syndrome
|
|
Hlhs - [Hypoplastic Left Heart Syndrome]
|
Hypoplasia Of Aortic Valve, In Hypoplastic Left Heart Syndrome
|
|
Atresia Of Mitral Valve, In Hypoplastic Left Heart Syndrome
|
Atresia Or Marked Hypoplasia Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle
|
|
Atresia Or Marked Hypoplasia, Of Aortic Orifice Or Valve, With Hypoplasia Of Ascending Aorta And Defective Development Of Left Ventricle With Mitral Valve Atresia
|
Aortic Valve Atresia, In Hypoplastic Left Heart Syndrome
|
|
Ascending Aorta Hypoplasia, In Hypoplastic Left Heart Syndrome
|
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
| Gummatous Syphilis |
|
|
| Interstitial Lung Disease 2 |
|
Idiopathic Pulmonary Fibrosis
|
Ipf
|
|
Fibrocystic Pulmonary Dysplasia
|
Pulmonary Fibrosis, Idiopathic
|
|
Pulmonary Fibrosis, Idiopathic, Susceptibility To
|
Cryptogenic Fibrosing Alveolitis
|
|
ILD2
|
Idiopathic Pulmonary Fibrosis, Familial
|
|
Fibrosing Alveolitis, Cryptogenic
|
Uip
|
|
Fibrosing Alveolitis
|
Interstitial Pneumonitis, Usual
|
|
Familial Idiopathic Pulmonary Fibrosis
|
Idiopathic Fibrosing Alveolitis, Chronic Form
|
|
Usual Interstitial Pneumonia
|
Fibrosing Alveolitis Cryptogenic
|
|
Hamman-Rich Disease
|
Idiopathic Pulmonary Fibrosis Familial
|
|
Interstitial Pneumonitis Usual
|
Fibrosis Idiopathic Pulmonary
|
|
Fibrosis, Pulmonary, Idiopathic
|
Hamman-Rich Syndrome
|
|
Chronic Idiopathic Pulmonary Fibrosis
|
Acute Interstitial Pneumonia
|
|
Interstitial Pulmonary Fibrosis
|
Ipf - [Idiopathic Pulmonary Fibrosis]
|
|
Idiopathic Lung Fibrosis
|
Fibrosing Lung Disease
|
|
Pulmonary Fibrosis Nos
|
Fibrosing Pneumonitis
|
|
|
| Micronodular Basal Cell Carcinoma |
|
Skin Micronodular Basal Cell Carcinoma
|
Basal Cell Carcinoma, Micronodular
|
|
|
| Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3 |
|
Spondylocheirodysplasia, Ehlers-Danlos Syndrome-Like
|
Scd-Eds
|
|
EDSSPD3
|
Ehlers-Danlos Syndrome Spondylodysplastic Type 3
|
|
Ehlers-Danlos Syndrome, Spondylocheirodysplastic Type
|
Slc39a13-Related Spondylodysplastic Ehlers-Danlos Syndrome
|
|
Slc39a13-Related Speds
|
Slc39a13-Related Spondylodysplastic Eds
|
|
Spondylocheirodysplastic Ehlers-Danlos Syndrome
|
Speds-Slc39a13
|
|
Ehlers-Danlos Syndrome-Like Spondylocheirodysplasia
|
Ehlers-Danlos Syndrome, Spondylodysplastic, Type 3
|
|
|
| Atrial Heart Septal Defect |
|
Atrial Septal Defect
|
Atrial Septal Defects
|
|
Atrioseptal Defect
|
Auricular Septal Defect
|
|
Congenital Atrial Septal Defect
|
Interatrial Septal Defect
|
|
Interauricular Septal Defect
|
Heart Septal Defects, Atrial
|
|
Septal Defect, Atrial
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Patent Foramen Ovale |
|
Atrial Septal Defect Within Oval Fossa
|
Foramen Ovale Patent
|
|
Ostium Secundum Atrial Septal Defect
|
Atrial Septal Defect, Ostium Secundum Type
|
|
Foramen Ovale, Patent
|
Defect, Patent Or Persistent, Ostium Secundum
|
|
Ostium Secundum Type Atrial Septal Defect
|
Persistent Ostium Secundum
|
|
Asd Ostium Secundum Type
|
Ostium Secundum Asd
|
|
Osasd
|
Asd, Ostium Secundum Type
|
|
Pfo - [Patent Foramen Ovale]
|
Open Foramen Ovale
|
|
Open Oval Foramen
|
Persistent Foramen Ovale
|
|
Secundum Atrial Septal Defect
|
|
|
| Tetralogy Of Fallot |
|
TOF
|
Fallot Tetralogy
|
|
Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle
|
Tetrad Of Fallot
|
|
Fallot Tetrad
|
Fallot Disease
|
|
Fallot Complex
|
Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy
|
|
Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle
|
Interventricular Septal Defect, In Tetralogy Of Fallot
|
|
Ventricular Septal Defect With Obstructed Right Ventricular Outflow
|
Tof - [Tetralogy Of Fallot]
|
|
Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]
|
Pulmonary Atresia, Ventricular Septal Defect And Mapcas
|
|
Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
|
|
|
| Eye Disease |
|
Eye Diseases
|
Abnormality Of The Eye
|
|
Toxoplasma Oculopathy
|
|
|
| Leukemia, Acute Myeloid |
|
Acute Myeloid Leukemia
|
Leukemia, Acute Myelogenous
|
|
Acute Myelogenous Leukemia
|
AML
|
|
Leukemia, Acute Myeloid, Susceptibility To
|
Acute Myeloblastic Leukemia
|
|
Leukemia, Acute Myeloid, Reduced Survival In, Somatic
|
Acute Myeloid Leukaemia
|
|
Leukemia, Myelocytic, Acute
|
Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome
|
|
Secondary Aml
|
Acute Myelocytic Leukemia
|
|
Acute Myeloid Leukemia, Somatic
|
Leukemia, Acute Myeloid, Somatic
|
|
Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic
|
Acute Myeloblastic Leukaemia
|
|
Acute Myelogenous Leukaemia
|
Aml - Acute Myeloid Leukemia
|
|
Acute Myeloid Leukemia With Cebpa Somatic Mutations
|
Aml With Cebpa Somatic Mutations
|
|
Inherited Acute Myeloid Leukemia
|
Familial Aml
|
|
Inherited Aml
|
Pure Familial Aml
|
|
Pure Familial Acute Myeloid Leukemia
|
Secondary Acute Myeloid Leukemia
|
|
Therapy-Related Aml And Myelodysplastic Syndrome
|
Acute Myeloid Leukemia, Secondary
|
|
Acute Non-Lymphoblastic Leukemia
|
Acute Non-Lymphocytic Leukemia
|
|
Acute Biphenotypic Leukemia
|
Acute Undifferentiated Leukemia
|
|
Acute Myeloblastic Leukaemia With Multilineage Dysplasia
|
Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission
|
|
Acute Myeloid Leukaemia With Myelodysplasia-Related Features
|
|
|
| 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
|
|
|
| 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
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
