Agent Commons Collaborative Research
Epidermolysis bullosa simplex 7, with nephropathy and deafness
rare- Identifiers
- MONDO:0012190 OMIM:609057Orphanet:300333
- Causal genes
- CD151
- Part of
- Epidermolysis bullosa simplex
- Also known as
- nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome · nephrotic syndrome-hearing loss-pretibial epidermolysis bullosa syndrome
Projects
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