Catalog
Autosomal recessive basal epidermolysis bullosa simplex
No MMS code
Link to WHO Definition
Autosomal recessive basal epidermolysis bullosa simplex – http://id.who.int/icd/entity/1280217391
Forms of epidermolysis bullosa simplex with autosomal recessive inheritance involving predominantly keratin 5, keratin 14 and plectin.
Parents
Children
- Epidermolysis bullosa simplex, autosomal recessive due to exophilin 5 deficiency
- Epidermolysis bullosa simplex with muscular dystrophy
- Epidermolysis bullosa simplex with pyloric atresia
- Autosomal recessive epidermolysis bullosa simplex due to BP230 deficiency
- Epidermolysis bullosa simplex, migratory circinate
- Epidermolysis bullosa simplex, autosomal recessive keratin 14 deficiency