Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE
Cutaneous Bullous Amyloidosis
cutaneous porphyria
cutis laxa +
Defect in Hyaluronan Metabolism
Dowling-Degos disease +
dyschromatosis universalis hereditaria +
dyskeratosis congenita +
ectodermal dysplasia +
Ehlers-Danlos syndrome +
epidermolysis bullosa +
epidermolytic hyperkeratosis +
erythrokeratodermia variabilis +
Familial Behcet-Like Autoinflammatory Syndrome +
familial cold autoinflammatory syndrome +
Familial Reactive Perforating Collagenosis
geroderma osteodysplasticum
Hailey-Hailey disease
Hepatic Porphyrias +
Hereditary Autoinflammatory Diseases +
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash, arthritis, fatigue, and secondary AMYLOIDOSIS. Hereditary autoinflammatory diseases are associated with mutations in genes involved in regulation of normal inflammatory process and are not caused by AUTOANTIBODIES, or antigen specific T-LYMPHOCYTES.
Hereditary Sclerosing Poikiloderma +
Histiocytic Dermatoarthritis
hyaline fibromatosis syndrome
ichthyosis vulgaris +
Isolated Osteopoikilosis
Juvenile Spring Eruption of Ears
Keratolytic Winter Erythema
keratosis follicularis +
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma