epidermolysis bullosa https://rarediseases.info.nih.gov/diseases/6359/epidermolysis-bullosa https://www.malacards.org/card/epidermolysis_bullosa NCIT:C67383 ICD10WHO:Q81 MESH:D004820 MONDO:0006541 NANDO:1200234 EFO:1000690 ICD9:757.39 Wikipedia:Epidermolysis_bullosa epidermolysis bullosa DOID:2730 Epidermolysis bullosa (EB) is a group of genetic skin diseases that cause the skin to blister very easily. Blisters form in response to minor injuries or friction, such as rubbing or scratching. There are four main types of epidermolysis bullosa: dystrophic epidermolysis bullosa Epidermolysis bullosa simplex Junctional epidermolysis bullosa Kindler Syndrome Identifying the exact type can be hard because there are many subtypes of EB. Within each type or subtype, a person may be mildly or severely affected. The disease can range from being a minor inconvenience to completely disabling, and fatal in some cases. Most types of EB are inherited. The inheritance pattern may be autosomal dominant or autosomal recessive. Management involves protecting the skin, reducing friction against the skin, and keeping the skin cool. NANDO:2100284 SCTID:61003004 UMLS:C0014527 EB GARD:0006359 NANDO:2201000 MEDGEN:41832 ICD10CM:Q81 vesiculobullous skin disease