MeSH Treeview
Query gene list
257415
FAM133B
family with sequence similarity 133, member B
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High-scoring List
Neoplasms
Musculoskeletal Diseases
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Williams Syndrome
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Supravalvular
Williams Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Williams Syndrome
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Genetic Diseases, Inborn
Chromosome Disorders
Williams Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosomal Instability
Chromosome Fragility
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Database Center for Life Science
