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113811
COL17A1
COLLAGEN, TYPE XVII, ALPHA-1
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Stomatognathic Diseases
Stomatognathic System Abnormalities
Tooth Abnormalities
Tooth Diseases
Tooth Abnormalities
Eye Diseases
Conjunctival Diseases
Pemphigoid, Benign Mucous Membrane
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Pemphigoid Gestationis
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Chromosome Disorders
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Junctional
Stomatognathic System Abnormalities
Tooth Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Junctional
Infant, Newborn, Diseases
Severe Combined Immunodeficiency
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Epidermolysis Bullosa Dystrophica
Skin Diseases
Hair Diseases
Hypotrichosis
Alopecia
Skin Abnormalities
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Junctional
Skin Diseases, Genetic
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Junctional
Skin Diseases, Vesiculobullous
Epidermolysis Bullosa
Epidermolysis Bullosa Dystrophica
Epidermolysis Bullosa, Junctional
Pemphigoid, Benign Mucous Membrane
Pemphigoid, Bullous
Pemphigoid Gestationis
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Severe Combined Immunodeficiency
Immune System Diseases
Autoimmune Diseases
Pemphigoid, Bullous
Immunologic Deficiency Syndromes
Severe Combined Immunodeficiency
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Alopecia
Atrophy
Nails, Malformed
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
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