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131900
EBS2
EPIDERMOLYSIS BULLOSA SIMPLEX, KOEBNER TYPE
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Genetic Diseases, Inborn
Chromosome Disorders
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Skin and Connective Tissue Diseases
Skin Diseases
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Chromosomal Instability
Chromosome Fragility
Genomic Instability
Chromosomal Instability
Chromosome Fragility
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