| KRT5 | |
| Gene ID | 3852 |
| Gene Symbol | KRT5 |
| Gene Name | keratin 5 |
| Organism | human |
| Phenotype from JST bibliography | epidermolysis bullosa simplex (MeSH) |
| MeSH Tree | Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Congenital Abnormalities > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex Skin and Connective Tissue Diseases > Skin Diseases > Skin Abnormalities > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Vesiculobullous > Epidermolysis Bullosa > Epidermolysis Bullosa Simplex |
| JST bibliography database | 06A0418068 |