This is just here as a test because I lose it
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has material basis in germline mutation in
- epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive
- Naegeli-Franceschetti-Jadassohn syndrome
- dermatopathia pigmentosa reticularis
- epidermolysis bullosa simplex 1A, generalized severe
- epidermolysis bullosa simplex 1C, localized
- epidermolysis bullosa simplex 1B, generalized intermediate