Annotation Detail
Information
- Associated Genes
- ZNF469
- Associated Variants
-
ZNF469 MUTATION
ZNF469 MUTATION - Associated Disease
- keratoconus
- Source Database
- DisGeNET
- Description
- Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus.
- Pubmed
- 25564447
- 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
- DisGENET score for the Gene Disease association
- 0.00108576748832121
Drugs