Annotation Detail
Information
- Associated Genes
- LOC102724652
- Associated Variants
-
LOC102724652 MUTATION
LOC102724652 MUTATION - Associated Disease
- CATARACT, MARNER TYPE
- Source Database
- DisGeNET
- Description
- A novel 3-base pair deletion of the CRYAA gene identified in a large Chinese pedigree featuring autosomal dominant congenital perinuclear cataract.
- Pubmed
- 25729975
- 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
- 0.000271441872080303
Drugs