Liver Cirrhosis, Experimental
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Abortion, Spontaneous
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Liver Cirrhosis
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Osteoarthritis
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Endometriosis
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Hypertension
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Muscular Dystrophy, Facioscapulohumeral
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Colorectal Cancer
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Keloid
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Rheumatoid Arthritis
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Craniofacial Abnormalities
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Prostatic Neoplasms
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Pulmonary Fibrosis
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Aortic Valve Insufficiency
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Mammary Neoplasms, Animal
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Mammary Neoplasms, Experimental
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Schizophrenia
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Melanoma
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Left Ventricular Hypertrophy
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Nephrotic Syndrome
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Carcinoma
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Fibrosis
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Ehlers-Danlos Syndrome Type 1
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Diabetic Nephropathy
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Megaepiphyseal Dwarfism
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Osteoporosis
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Mesothelioma, Malignant
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Hyperglycemia
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Hyperinsulinism
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Drug-Induced Liver Injury
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Leiomyoma, Epithelioid
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Breast Carcinoma
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Glioblastoma Multiforme
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Neoplasm Invasiveness
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Osteogenesis Imperfecta, Type 2a
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Osteogenesis Imperfecta, Type 3
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Hearing Loss, Sensorineural
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Alport Syndrome, Recessive Type
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Heart Valve Diseases
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Focal Segmental Glomerulosclerosis
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Ehlers-Danlos Syndrome, Type Vii, Autosomal Dominant
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Osteochondrodysplasias
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Intervertebral Disc Disease
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Osteogenesis Imperfecta, Type 4
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Oral Submucous Fibrosis
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Marfan Syndrome
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Varicose Veins
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Ulcerative Colitis
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Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
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Erythema
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Fatty Liver
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Femur Head Necrosis
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Fractures, Bone
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Glaucoma, Angle-Closure
|
Glioma
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Glomerulopathy With Fibronectin Deposits
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Hematuria, Benign Familial
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Hernia, Diaphragmatic
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Hyaloideoretinal Degeneration Of Wagner
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Hypercholesterolemia
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Hyperostosis, Cortical, Congenital
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Hyperplasia
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Inflammation
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Intellectual Disability
|
Intervertebral Disc Displacement
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Joint Instability
|
Kallmann Syndrome
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Keutel Syndrome
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Kniest Dysplasia
|
Legg-Calve-Perthes Disease
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Leiomyomatosis, Esophageal And Vulval, With Nephropathy
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Leukemia, Myeloid, Acute
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Limb Deformities, Congenital
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Alcoholic Liver Cirrhosis
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Liver Diseases
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Lung Injury
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Marshall Syndrome
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Mass Syndrome
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Metaphyseal Chondrodysplasia Schmid Type
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Mouth Neoplasms
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Cardiomyopathy, Dilated, 3b
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Myocardial Ischemia
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Myopia
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Neoplasm Metastasis
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Alport Syndrome, X-Linked
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Nephrogenic Fibrosing Dermopathy
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Nerve Degeneration
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Non-Alcoholic Fatty Liver Disease
|
Osteoarthritis With Mild Chondrodysplasia
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Osteogenesis Imperfecta
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Osteomalacia
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Ovarian Cysts
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Pancreatic Carcinoma
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Pelvic Organ Prolapse
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Pierre Robin Syndrome With Fetal Chondrodysplasia
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Platyspondylic Lethal Skeletal Dysplasia, Torrance Type
|
Pleural Diseases
|
Pneumoconiosis
|
Porencephaly
|
Pseudoachondroplasia
|
Chronic Obstructive Pulmonary Disease
|
Pulmonary Emphysema
|
Retinal Detachment
|
Cone-Rod Dystrophy 2
|
Retinitis Pigmentosa 25
|
Rupture, Spontaneous
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Systemic Scleroderma
|
Shprintzen Golberg Craniosynostosis
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Small Cell Lung Carcinoma
|
Spondyloepimetaphyseal Dysplasia, Aggrecan Type
|
Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related
|
Spondyloepiphyseal Dysplasia, Congenita
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Spondyloepiphyseal Dysplasia, Kimberley Type
|
Spondylometaphyseal Dysplasia, Kozlowski Type
|
Stickler Syndrome, Type 1
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Stickler Syndrome, Type 2
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Stickler Syndrome, Type 3
|
Stickler Syndrome, Type I, Nonsyndromic Ocular
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Stiff Skin Syndrome
|
Stomach Neoplasms
|
Strudwick Syndrome
|
Synovitis
|
Synpolydactyly 2
|
Uremia
|
Ureteral Obstruction
|
Vascular Calcification
|
Weight Gain
|
Weight Loss
|
Weill-Marchesani Syndrome
|
Williams Syndrome
|
Wounds And Injuries
|
Achondrogenesis Type 2
|
Aids-Related Opportunistic Infections
|
Aneurysm, Dissecting
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Angiopathy, Hereditary, With Nephropathy, Aneurysms, And Muscle Cramps
|
Thoracic Aortic Aneurysm
|
Aortic Diseases
|
Aortic Rupture
|
Aortic Stenosis, Supravalvular
|
Arachnodactyly
|
Arthritis
|
Arthritis, Experimental
|
Asthma
|
Autism
|
Autoimmune Disease
|
Brain Small Vessel Disease With Hemorrhage
|
Calcinosis
|
Hepatocellular Carcinoma
|
Squamous Cell Carcinoma
|
Cartilage Diseases
|
Cataract
|
Cell Transformation, Neoplastic
|
Cholangitis
|
Chondrosarcoma
|
Coloboma
|
Corneal Dystrophy, Fuchs' Endothelial, 1
|
Corneal Dystrophy, Posterior Polymorphous, 1
|
Corneal Dystrophy, Posterior Polymorphous, 2
|
Crohn's Disease
|
Cutis Laxa
|
Deafness, Autosomal Dominant 12
|
Deafness, Autosomal Dominant 13
|
Deafness, Autosomal Dominant 39, With Dentinogenesis Imperfecta 1
|
Deafness, Autosomal Recessive 21
|
Deafness, Autosomal Recessive 53
|
Dentinogenesis Imperfecta
|
Dentinogenesis Imperfecta, Shields Type 3
|
Diabetes Mellitus
|
Ectopia Lentis
|
Edema
|
Ehlers-Danlos Syndrome
|
Ehlers-Danlos Syndrome, Cardiac Valvular Form
|
Ehlers-Danlos Syndrome Type 2
|
Ehlers-Danlos Syndrome Type 3
|
Endomyocardial Fibrosis
|
Epiphyseal Dysplasia, Multiple, 1
|
Epiphyseal Dysplasia, Multiple, 3
|
Epiphyseal Dysplasia, Multiple, 5
|