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Query OMIM entry list
125635
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DERMOGRAPHISM, FAMILIAL
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Genetic Diseases, Inborn
Chromosome Disorders
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Vascular
Urticaria
Immune System Diseases
Hypersensitivity
Hypersensitivity, Delayed
Hypersensitivity, Immediate
Urticaria
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
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