Annotation Detail
Information
- Associated Genes
- ITM2B
- Associated Variants
-
ITM2B MUTATION
ITM2B MUTATION - Associated Disease
- RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES
- Source Database
- DisGeNET
- Description
- NA
- Original source reporting the Gene Disease association
- ORPHANET,UNIPROT
- DisGENET score for the Gene Disease association
- 0.24
Drugs