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134797
FBN1
FIBRILLIN 1
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Craniosynostoses
Marfan Syndrome
Hand Deformities
Hand Deformities, Congenital
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Limb Deformities, Congenital
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Synostosis
Craniosynostoses
Nervous System Diseases
Neuromuscular Diseases
Muscular Diseases
Muscular Disorders, Atrophic
Muscular Dystrophies
Eye Diseases
Corneal Diseases
Eye Abnormalities
Ectopia Lentis
Eye Diseases, Hereditary
Gyrate Atrophy
Lens Diseases
Cataract
Lens Subluxation
Ectopia Lentis
Ocular Hypertension
Glaucoma
Uveal Diseases
Choroid Diseases
Gyrate Atrophy
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Marfan Syndrome
Heart Diseases
Cardiomyopathies
Heart Defects, Congenital
Heart Septal Defects
Marfan Syndrome
Heart Valve Diseases
Aortic Valve Insufficiency
Aortic Valve Stenosis
Heart Valve Prolapse
Mitral Valve Prolapse
Ventricular Outflow Obstruction
Aortic Valve Stenosis
Vascular Diseases
Aneurysm
Aneurysm, Dissecting
Aortic Aneurysm
Aortic Aneurysm, Thoracic
Aortic Diseases
Aortic Aneurysm
Aortic Aneurysm, Thoracic
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Marfan Syndrome
Eye Abnormalities
Ectopia Lentis
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Limb Deformities, Congenital
Hand Deformities, Congenital
Synostosis
Craniosynostoses
Skin Abnormalities
Genetic Diseases, Inborn
Eye Diseases, Hereditary
Gyrate Atrophy
Marfan Syndrome
Muscular Dystrophies
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Scleroderma, Systemic
Skin Diseases
Scleroderma, Systemic
Skin Abnormalities
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Dilatation, Pathologic
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Emphysema
Fibrosis
Growth Disorders
Database Center for Life Science
