| Disease ID | Source | Name | Description |
| 226600 | OMIM | Epidermolysis bullosa dystrophica, autosomal recessive (RDEB) | A group of autosomal recessive blistering skin diseases characterized by tissue separation which occurs below the dermal-epidermal basement membrane at the level of the anchoring fibrils. Various clinical types with different severity are recognized, ranging from severe mutilating forms, such as epidermolysis bullosa dystrophica Hallopeau-Siemens type, to mild forms with limited localized scarring and less frequent extracutaneous manifestations. Mild forms include epidermolysis bullosa mitis and epidermolysis bullosa localisata. The disease is caused by variants affecting the gene represented in this entry. |
| 131705 | OMIM | Transient bullous dermolysis of the newborn (TBDN) | TBDN is a neonatal form of dystrophic epidermolysis bullosa characterized by sub-epidermal blisters, reduced or abnormal anchoring fibrils at the dermo-epidermal junction, and electron-dense inclusions in keratinocytes. TBDN heals spontaneously or strongly improves within the first months and years of life. The disease is caused by variants affecting the gene represented in this entry. |
| 131750 | OMIM | Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) | A group of autosomal dominant blistering skin diseases characterized by tissue separation which occurs below the dermal-epidermal basement membrane at the level of the anchoring fibrils. Various clinical types with different severity are recognized, ranging from severe mutilating forms to mild forms with limited and localized scarring, and less frequent extracutaneous manifestations. The disease is caused by variants affecting the gene represented in this entry. |
| 131750 | OMIM | Epidermolysis bullosa dystrophica, autosomal dominant (DDEB) | A group of autosomal dominant blistering skin diseases characterized by tissue separation which occurs below the dermal-epidermal basement membrane at the level of the anchoring fibrils. Various clinical types with different severity are recognized, ranging from severe mutilating forms to mild forms with limited and localized scarring, and less frequent extracutaneous manifestations. The disease is caused by variants affecting the gene represented in this entry. |
| 131850 | OMIM | Epidermolysis bullosa dystrophica, pretibial type (PR-DEB) | A form of dystrophic epidermolysis bullosa characterized by pretibial blisters that develop into prurigo-like hyperkeratotic lesions. It predominantly affects the pretibial areas, sparing the knees and other parts of the skin. Other clinical features include nail dystrophy, albopapuloid skin lesions, and hypertrophic scars without pretibial predominance. The phenotype shows considerable interindividual variability. Inheritance is autosomal dominant. The disease is caused by variants affecting the gene represented in this entry. |
| 132000 | OMIM | Epidermolysis bullosa dystrophica, Bart type (B-DEB) | An autosomal dominant form of dystrophic epidermolysis bullosa characterized by congenital localized absence of skin, skin fragility and deformity of nails. The disease is caused by variants affecting the gene represented in this entry. |
| 604129 | OMIM | Epidermolysis bullosa pruriginosa (EBP) | A distinct clinical subtype of epidermolysis bullosa dystrophica. It is characterized by skin fragility, blistering, scar formation, intense pruritus and excoriated prurigo nodules. Onset is in early childhood, but in some cases is delayed until the second or third decade of life. Inheritance can be autosomal dominant or recessive. The disease is caused by variants affecting the gene represented in this entry. |
| 607523 | OMIM | Nail disorder, non-syndromic congenital, 8 (NDNC8) | A nail disorder characterized by isolated toenail dystrophy. The nail changes are most severe in the great toes and consist of the nail plate being buried in the nail bed with a deformed and narrow free edge. The disease is caused by variants affecting the gene represented in this entry. |