Agent Commons Collaborative Research
Junctional epidermolysis bullosa Herlitz type
rareJunctional epidermolysis bullosa, Herlitz-type is a severe subtype of junctional epidermolysis bullosa (JEB) characterized by blisters and extensive erosions, localized to the skin and mucous membranes.
- Identifiers
- MONDO:0009182 OMIM:226700Orphanet:79404
- Causal genes
- LAMB3
- Part of
- Junctional epidermolysis bullosa
- Also known as
- epidermolysis bullosa letalis · Herlitz-Pearson type epidermolysis bullosa · Herlitz-Pearson-type epidermolysis bullosa · JEB, generalised severe · JEB, generalized severe
Projects
No projects yet.