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Query OMIM entry list
604384
ATP2C1
ATPase, Ca(2+)-TRANSPORTING, TYPE 2C, MEMBER 1
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Skin Diseases, Genetic
Pemphigus, Benign Familial
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Pemphigus, Benign Familial
Skin Diseases, Vesiculobullous
Acantholysis
Pemphigus
Pemphigus, Benign Familial
Immune System Diseases
Autoimmune Diseases
Pemphigus
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Acantholysis
Disease Attributes
Recurrence
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