| Diseases |
Alias |
|
| Corneal Dystrophy, Congenital Stromal |
|
Congenital Stromal Corneal Dystrophy
|
CSCD
|
|
Congenital Hereditary Stromal Dystrophy
|
Congenital Hereditary Stromal Dystrophy Of The Cornea
|
|
Congenital Stromal Dystrophy Of The Cornea
|
Dacs
|
|
Decorin-Associated Congenital Stromal Corneal Dystrophy
|
Dystrophia Corneae Parenchymatosa Congenita
|
|
Witschel Dystrophy
|
Dystrophy, Corneal, Stromal, Congenital
|
|
|
| Stromal Corneal Dystrophy |
|
Stromal Dystrophies Corneal
|
|
|
| Localized Scleroderma |
|
Morphea
|
Localised Scleroderma
|
|
Localized Fibrosing Scleroderma
|
Circumscribed Scleroderma
|
|
Localised Morphea
|
Localised Morphoea
|
|
Localized Morphea
|
Scleroderma, Circumscribed Or Localised
|
|
Scleroderma, Circumscribed Or Localized
|
Scleroderma, Localized
|
|
|
| Corneal Dystrophy |
|
|
| Pseudoachondroplasia |
|
PSACH
|
Pseudoachondroplastic Dysplasia
|
|
Pseudoachondroplastic Spondyloepiphyseal Dysplasia Syndrome
|
Spondyloepiphyseal Dysplasia, Pseudoachondroplastic
|
|
Pseudoachondroplastic Spondyloepiphyseal Dysplasia
|
Spondyloepiphyseal Dysplasia Pseudoachondroplastic
|
|
|
| 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
|
|
|
| Neonatal Marfan Syndrome |
|
|
| Gingival Overgrowth |
|
Gingival Enlargement
|
Gingival Hyperplasia
|
|
Gingival Bulge
|
Gingival Enlargement Nos
|
|
Gingival Hypertrophy
|
Gum Hypertrophy
|
|
Hyperplasia Gum
|
Gingival Thickening
|
|
Hyperplasia Of Gingiva
|
Hypertrophy Of Gingiva
|
|
Hypertrophy Of Mucous Membrane Of Gums
|
|
|
| Ehlers-Danlos Syndrome |
|
Eds
|
Cutis Hyperelastica
|
|
Elastic Skin
|
Ehlers-Danlos Syndromes
|
|
Ed Syndrome
|
Ehlers Danlos Syndrome
|
|
Ehlers Danlos Disease
|
Eds - [Ehlers-Danlos Syndrome]
|
|
|
| Bullous Keratopathy |
|
Bk - [Bullous Keratopathy]
|
|
|
| Crouzon Syndrome |
|
Crouzon Craniofacial Dysostosis
|
Craniofacial Dysostosis
|
|
Cfd1
|
Craniofacial Dysostosis Type 1
|
|
Crouzon Disease
|
Crouzon'S Disease
|
|
Craniofacial Dysostosis, Type I
|
Craniofacial Dysarthrosis
|
|
Craniofacial Dysostosis Syndrome
|
CS
|
|
Craniofacial Dysostosis Type I
|
Vogt Cephalosyndactyly
|
|
|
| Cornea Plana |
|
|
| Tendinopathy |
|
|
| Osteoarthritis |
|
Osteoarthrosis
|
Degenerative Joint Disease
|
|
Hypertrophic Arthritis
|
Arthropathy
|
|
Degenerative Polyarthritis
|
Degenerative Arthritis
|
|
Osteoarthrosis And Allied Disorder
|
Arthritis, Degenerative
|
|
Oa
|
Osteoarthritis Deformans
|
|
Osteoarthrosis Deformans
|
Kashin-Beck Disease
|
|
|
| Stromal Dystrophy |
|
|
| Pulmonary Fibrosis |
|
|
| 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
|
|
|
| Scleredema Adultorum |
|
Scleredema
|
Buschke'S Scleredema
|
|
Scleredema Adultorum Of Buschke
|
Scleredema Diabeticorum
|
|
Scleredema Diabeticorum Of Buschke
|
Buschke Scleredema
|
|
|
| Peyronie'S Disease |
|
Induratio Penis Plastica
|
Peyronie Disease
|
|
Peyronies Disease
|
Peyronie'S Fibromatosis
|
|
Penile Induration
|
Balanitis Xerotica Obliterans
|
|
|
| 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]
|
|
|
| Myopia |
|
Near-Sightedness
|
Short-Sightedness
|
|
Nearsightedness
|
Nearsighted
|
|
Near Vision
|
Close Sighted
|
|
Myopic
|
Short-Sighted
|
|
Near Sighted
|
|
|
| Recessive Dystrophic Epidermolysis Bullosa |
|
Autosomal Recessive Dystrophic Epidermolysis Bullosa Generalisata Gravis
|
Autosomal Recessive Dystrophic Epidermolysis Bullosa, Hallopeau-Siemens Type
|
|
Rdeb, Hallopeau-Siemens Type
|
Severe Generalized Rdeb
|
|
Severe Generalized Recessive Dystrophic Epidermolysis Bullosa
|
Rdeb Generalisata Gravis
|
|
Rdeb, Severe Generalized
|
Rdeb-Sev Gen
|
|
Recessive Dystrophic Epidermolysis Bullosa, Severe Generalized
|
Hallopeau-Siemens Disease
|
|
|
| Saul-Wilson Syndrome |
|
Microcephalic Osteodysplastic Dysplasia
|
Microcephalic Osteodysplastic Dysplasia, Saul-Wilson Type
|
|
SWILS
|
Microcephalic Osteodysplastic Dysplasia Saul Wilson Type
|
|
|
| Glomerulonephritis |
|
|
| Macular Dystrophy, Corneal |
|
Macular Corneal Dystrophy
|
MCD
|
|
Corneal Dystrophy, Macular Type
|
Groenouw Type Ii Corneal Dystrophy
|
|
Fehr Corneal Dystrophy
|
Macular Dystrophy, Corneal Type 1
|
|
Mcdc1
|
Macular Corneal Dystrophy Type Ii
|
|
Macular Corneal Dystrophy, Type Ii
|
Macular Corneal Dystrophy, Type I
|
|
Mcdc1, Formerly
|
Macular Dystrophy, Corneal, 1
|
|
Macular Corneal Dystrophy Type 1
|
Corneal Dystrophy Groenouw Type Ii
|
|
Corneal Dystrophy Macular Type
|
Macular Corneal Dystrophy Type I
|
|
Dystrophy, Macular, Corneal
|
|
|
| Acrodermatitis Chronica Atrophicans |
|
Acrodermatitis Atrophicans Chronica
|
Herxheimer Disease
|
|
Primary Diffuse Atrophy
|
|
|
| Corneal Dystrophy, Posterior Amorphous |
|
Posterior Amorphous Corneal Dystrophy
|
PACD
|
|
Chromosome 12q21.33 Deletion Syndrome
|
Posterior Amorphous Stromal Dystrophy
|
|
|
| Secondary Corneal Edema |
|
|
| Tendinitis |
|
|
| 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
|
|
|
| Epicondylitis |
|
Tennis Elbow
|
Lateral Epicondylitis
|
|
Golfer'S Elbow
|
Medial Epicondylitis
|
|
Andrel Epicondylitis
|
Archer'S Elbow
|
|
Hockey Elbow
|
Shooter'S Elbow
|
|
|
| Spondyloepiphyseal Dysplasia With Congenital Joint Dislocations |
|
Spondyloepiphyseal Dysplasia
|
Chst3-Related Skeletal Dysplasia
|
|
Humerospinal Dysostosis
|
Spondyloepiphyseal Dysplasia, Omani Type
|
|
Chondrodysplasia With Multiple Dislocations
|
SEDCJD
|
|
Hsd
|
Cdmd
|
|
Humero-Spinal Dysostosis
|
Kozlowski Celermajer Tink Syndrome
|
|
Chondrodysplasia With Congenital Joint Dislocations, Chst3 Type
|
Larsen Syndrome, Recessive Type
|
|
Humero-Spinal Dysostosis With Congenital Heart Disease
|
Omani Type
|
|
Sed
|
Chst3 Deficiency
|
|
Chst3-Related Dysplasia
|
Recessive Larsen Syndrome
|
|
Autosomal Recessive Larsen Syndrome
|
Sed With Luxations, Chst3 Type
|
|
Sed, Omani Type
|
Sdcd, Chst3 Type
|
|
Spondyloepiphyseal Dysplasia With Congenital Joint Dyslocations, Chst3 Type
|
Sed Omani Type
|
|
Spondyloepiphyseal Dysplasia Omani Type
|
Larsen Syndrome, Autosomal Recessive
|
|
Mucopolysaccharidosis Iv
|
Spondyloepiphyseal Dysplasia, Congenita
|
|
|
| Collagen Disease |
|
Collagen Diseases
|
Collagen Disorder
|
|
|
| Pre-Eclampsia |
|
Preeclampsia
|
Gestational Hypertension
|
|
Hypertension Induced By Pregnancy
|
Pre-Eclamptic Toxaemia
|
|
Pregnancy Associated Hypertension
|
Proteinuric Hypertension Of Pregnancy
|
|
Hypertension, Pregnancy-Induced, Susceptibility To
|
Preeclampsia/Eclampsia
|
|
Pregnancy Toxemia
|
Toxaemia Of Pregnancy
|
|
Gestational Proteinuric Hypertension
|
Pregnancy-Induced Hypertension
|
|
Toxemia Of Pregnancy
|
Preeclampsia, Susceptibility To
|
|
Transient Hypertension Of Pregnancy
|
Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria
|
|
Gestational Hypertension Nos
|
Mild Proteinuric Hypertension Of Pregnancy
|
|
Pih - [Pregnancy-Induced Hypertension]
|
Pregnancy-Induced Hypertension Nos
|
|
Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria
|
Pe - [Pre-Eclampsia]
|
|
Pre-Eclampsia Nos
|
Pre-Eclamptic Nos
|
|
Pregnancy Pre-Eclampsia
|
Puerperal Pre-Eclampsia
|
|
Pre-Eclampsia Toxaemia
|
Toxaemia In Pregnancy
|
|
Pet - [Pre-Eclamptic Toxaemia]
|
Maternal Toxaemia
|
|
|
| Bethlem Myopathy 1 |
|
Bethlem Myopathy
|
Myopathy, Benign Congenital, With Contractures
|
|
Muscular Dystrophy, Benign Congenital
|
BTHLM1
|
|
Muscular Dystrophy, Limb-Girdle, Autosomal Dominant 5
|
Lgmdd5
|
|
Benign Congenital Muscular Dystrophy
|
Benign Autosomal Dominant Myopathy
|
|
Myopathy, Bethlem
|
Myopathy, Bethlem, Type 1
|
|
|
| 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
|
|
|
| Cervical Incompetence |
|
Uterine Cervical Incompetence
|
|
|
| Achondrogenesis |
|
|
| Scoliosis |
|
|
| Ullrich Congenital Muscular Dystrophy 1 |
|
Ullrich Congenital Muscular Dystrophy
|
Ullrich Disease
|
|
Ucmd
|
Ullrich Scleroatonic Muscular Dystrophy
|
|
Scleroatonic Muscular Dystrophy
|
UCMD1
|
|
Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 22
|
Lgmdr22
|
|
Muscular Dystrophy, Scleroatonic
|
Late Onset Scleroatonic Familial Myopathy
|
|
Congenital Muscular Dystrophy, Ullrich Type
|
|
|
| Geroderma Osteodysplasticum |
|
Gerodermia Osteodysplastica
|
Geroderma Osteodysplastica
|
|
GO
|
Walt Disney Dwarfism
|
|
Type Of Gerodermia Osteodysplastica
|
|
|
| Spinocerebellar Ataxia 38 |
|
Spinocerebellar Ataxia Type 38
|
SCA38
|
|
Ataxia, Spinocerebellar, Type 38
|
|
|
| Corneal Disease |
|
Corneal Diseases
|
Corneal Disorders
|
|
|
| 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
|
|
|
| Epidermolysis Bullosa Dystrophica |
|
Dystrophic Epidermolysis Bullosa
|
Deb
|
|
Dermolytic Epidermolysis Bullosa
|
Epidermolysis Bullosa, Dermolytic
|
|
Epidermolysis Bullosa, Dystrophic
|
Epidermolysis Bullosa Dystrophic
|
|
Dystrophic Eb - [Epidermolysis Bullosa]
|
|
|
| Preterm Premature Rupture Of The Membranes |
|
Preterm Premature Rupture Of Membranes
|
PPROM
|
|
Preterm Premature Rupture Of The Membranes, Susceptibility To
|
Pprom - [Preterm Premature Rupture Of Membranes]
|
|
Preterm Rupture Of Membranes
|
|
|
| Ovarian Cancer |
|
Ovarian Carcinoma
|
Ovarian Neoplasm
|
|
Malignant Tumour Of Ovary
|
Cancer Of The Ovary
|
|
Epithelial Ovarian Cancer
|
Neoplasm Of Ovary
|
|
Ovarian Neoplasms
|
Ovarian Cancers
|
|
Malignant Neoplasm Of Ovary
|
Primary Malignant Neoplasm Of Ovary
|
|
Ovarian Cancer, Somatic
|
Malignant Ovarian Tumor
|
|
Ovary Neoplasm
|
Primary Ovarian Cancer
|
|
Tumor Of The Ovary
|
Malignant Neoplasm Of The Ovary
|
|
Malignant Tumor Of The Ovary
|
Ovarian Malignant Tumor
|
|
OC
|
Ovarian Carcinomas
|
|
Cancer, Ovarian
|
Cancer Of Ovary
|
|
Ovary Cancer
|
Ca Ovary
|
|
|
| Muscular Dystrophy, Duchenne Type |
|
Duchenne Muscular Dystrophy
|
DMD
|
|
Muscular Dystrophy, Duchenne
|
Muscular Dystrophy, Pseudohypertrophic Progressive, Duchenne Type
|
|
Severe Dystrophinopathy, Duchenne Type
|
Muscular Dystrophy Duchenne
|
|
Dystrophy, Muscular, Duchenne Type
|
Benign Duchenne Muscular Dystrophy
|
|
Duchenne Motor Neuron Disease
|
Duchenne Type Dystrophy
|
|
Duchenne-Griesinger Disease
|
|
|
| Osteogenic Sarcoma |
|
Osteosarcoma
|
OSRC
|
|
Osteosarcoma, Somatic
|
Neoplasms, Bone Tissue
|
|
Bone Tissue Neoplasm
|
Osteoid Sarcoma
|
|
Skeletal Sarcoma
|
Osteosarcoma Of Bone
|
|
Bone Sarcoma
|
|
|
| Hyperinsulinemic Hypoglycemia, Familial, 1 |
|
HHF1
|
Persistent Hyperinsulinemic Hypoglycemia Of Infancy
|
|
Familial Hyperinsulinemic Hypoglycemia 1
|
Congenital Hyperinsulinism
|
|
Phhi
|
Autosomal Dominant Hyperinsulinism Due To Sur1 Deficiency
|
|
Hypoglycemia, Hyperinsulinemic, Of Infancy
|
Hyperinsulinemic Hypoglycemia Due To Focal Adenomatous Hyperplasia
|
|
Nesidioblastosis Of Pancreas
|
Hyperinsulinism, Familial, With Pancreatic Nesidioblastosis
|
|
Hyperinsulinism, Congenital
|
Autosomal Dominant Hyperinsulinemic Hypoglycemia Due To Sur1 Deficiency
|
|
Diazoxide-Resistant Focal Hyperinsulinism Due To Sur1 Deficiency
|
Hyperinsulinemic Hypoglycemia Due To Sur1 Deficiency, Diazoxide-Resistant Focal Form
|
|
Autosomal Recessive Hyperinsulinism Due To Sur1 Deficiency
|
Autosomal Recessive Hyperinsulinemic Hypoglycemia Due To Sur1 Deficiency
|
|
Hypoglycemia, Hyperinsulinemic, Familial, Type 1
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Cancer Of The Pancreas
|
Pancreatic Carcinoma, Somatic
|
|
Pancreatic Cancer, Somatic
|
Ca Body Of Pancreas
|
|
Ca Head Of Pancreas
|
Ca Tail Of Pancreas
|
|
Malignant Neoplasm Of Body Of Pancreas
|
Malignant Neoplasm Of Head Of Pancreas
|
|
Malignant Neoplasm Of Tail Of Pancreas
|
Pancreas Neoplasm
|
|
Exocrine Cancer
|
Exocrine Pancreas Carcinoma
|
|
Hereditary Pancreatic Cancer
|
Hereditary Pancreatic Carcinoma
|
|
PNCA
|
Pancreatic Cancer, Susceptibility To
|
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| 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
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Fuchs' Endothelial Dystrophy |
|
Fuchs Endothelial Corneal Dystrophy
|
Fuchs Endothelial Dystrophy
|
|
Fuchs Dystrophy
|
Fced
|
|
Fuchs' Corneal Dystrophy
|
Fuchs' Endothelial Corneal Dystrophy
|
|
Fuchs Atrophy
|
Fuchs Corneal Dystrophy
|
|
Endoepithelial Corneal Dystrophy
|
Fecd
|
|
Late Hereditary Endothelial Dystrophy
|
Corneal Dystrophy, Fuchs Endothelial
|
|
Dystrophy, Corneal, Fuchs Endothelial
|
Corneal Dystrophy, Fuchs' Endothelial, 1
|
|
|
| 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
|
|
|
| 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
|
|
|
