MeSH Treeview
Query OMIM entry list
146590
IHCM
ICHTHYOSIS HYSTRIX, CURTH-MACKLIN TYPE
→
High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Skin Abnormalities
Epidermolysis Bullosa
Ichthyosis
Genetic Diseases, Inborn
Skin Diseases, Genetic
Epidermolysis Bullosa
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Infant, Newborn, Diseases
Ichthyosis
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Pigmentation Disorders
Hyperpigmentation
Skin Abnormalities
Epidermolysis Bullosa
Ichthyosis
Skin Diseases, Genetic
Epidermolysis Bullosa
Keratoderma, Palmoplantar
Keratoderma, Palmoplantar, Diffuse
Skin Diseases, Vesiculobullous
Acantholysis
Epidermolysis Bullosa
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Acantholysis
Database Center for Life Science
