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Query OMIM entry list
169900
PEPB
PEPTIDASE B
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Hyperpigmentation
Skin Diseases, Genetic
Skin Diseases, Vesiculobullous
Acantholysis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Acantholysis
Database Center for Life Science
