In the demo data, load the clinical note and all phenotype terms, then click the edit button
then remove a few terms (here I removed "difficulty walking" from all sources)
And it's not clear what to do next. The "close" button is deactivated and it's unclear whether the list has been updated. So I just closed the window with the (X)
We should make this more clear to the user that the gene list has been updated to reflect the change in terms
In the demo data, load the clinical note and all phenotype terms, then click the edit button
then remove a few terms (here I removed "difficulty walking" from all sources)
And it's not clear what to do next. The "close" button is deactivated and it's unclear whether the list has been updated. So I just closed the window with the (X)
We should make this more clear to the user that the gene list has been updated to reflect the change in terms