Junctional epidermolysis bullosa inversa is a rare severe subtype of junctional epidermolysis bullosa (JEB) characterized by blistering and erosions confined to intertriginous skin sites, the esophagus, and vagina.
Comprehensive, easy-to-understand information about this condition
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late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome
MONDO:0009177
junctional epidermolysis bullosa, non-Herlitz type
MONDO:0009180
junctional epidermolysis bullosa Herlitz type
MONDO:0009182
junctional epidermolysis bullosa with pyloric atresia
MONDO:0009183
laryngo-onycho-cutaneous syndrome
MONDO:0009513
epidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome
MONDO:0013881