The current flow chart in the methods section needs to be updated.
TODO:
[x] normalize the figure style
[x] define high-evident genes as >= 2
[x] define low-evident genes as < = 1 (0 and 1) and explain evidence criteria = 0
[ ] implement 7. phenotype "metabolic kidney disorders (including monogenic urinary stone disorders)" as selection option in the group, even think about considering the 8 phenotypes regarding this publication: A Clinical Workflow for Cost-Saving High-Rate Diagnosis of Genetic Kidney Diseases
[x] correct first evidence criteria in the timeline after merging and add a new merged table
[x] give only 4 options for curated classes in the example Gene --> change Refuted to No-Known Disease Relationship
The current flow chart in the methods section needs to be updated.
TODO: