Disease #01310 (epidermolysis bullosa, simplex, simplex, Weber-Cockayne type, OMIM:131800)
Official abbreviation |
- |
Name |
epidermolysis bullosa, simplex, simplex, Weber-Cockayne type |
OMIM ID |
131800 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 3 genes |
ITGB4, KRT14, KRT5 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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