Annotation Detail
Information
- Associated Genes
- KRT10
- Associated Variants
-
KRT10 MUTATION
KRT10 MUTATION - Associated Disease
- Congenital reticular ichthyosiform erythroderma
- Source Database
- DisGeNET
- Description
- The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome.
- Pubmed
- 25210931
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree,CTD_human,ORPHANET
- DisGENET score for the Gene Disease association
- 0.241085767488321
Drugs