PedAM
Pediatric Disease Annotations & Medicines
| Disease | skin disease |
| Phenotype | C0020757|ichthyosis |
| Sentences | 1 |
| PubMedID- 20236940 | Recently, heterozygous loricrin gene mutations have been identified in two dominantly inherited skin diseases, vohwinkel syndrome with ichthyosis and progressive symmetric erythrokeratoderma, collectively termed loricrin keratoderma. |
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