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139350
KRT1
KERATIN 1
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Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Genetic Diseases, Inborn
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Infant, Newborn, Diseases
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Database Center for Life Science
