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600194
KRT2A
KERATIN 2A
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Stomatognathic Diseases
Mouth Diseases
Periodontal Diseases
Periodontitis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Infant, Newborn, Diseases
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Abnormalities
Ichthyosis
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Diseases, Genetic
Ichthyosiform Erythroderma, Congenital
Hyperkeratosis, Epidermolytic
Skin Diseases, Vesiculobullous
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
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