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Please remove Carlo, he's no longer with us, unfortunately.
For those of us labeled as PIs, perhaps change our bios to read "X is currently a PI of the Monarch Initiative...." that way we can all hav…
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Digeorge syndrome
http://tartini.crbs.ucsd.edu/disease/OMIM_188400
is listed as having two identical subclasses, which reroute to this page when clicked.
so, are they subclasses or equivalent?
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This should have a parameter that specifies the number of models to return by rank (default to 10). Because we have several scoring mechanisms, this will default to just one of them (maybe BMAasymIC)…
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@cmungall
Autocomplete has duplicate entries, for example search on
Choroidal degeneration
these are because of synonyms and equivalency axioms, however, since the landing page takes you to the cho…
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There are some things I need to complete pages:
1. Phenotype spotlight on Phenotype main page: This is currently "Large floppy ears." Please give me the link for a phenotype that you would like featur…
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http://tartini.crbs.ucsd.edu/phenotype/HP_0010788
wrong:
![screen shot 2014-02-06 at 4 32 46 pm](https://f.cloud.github.com/assets/50745/2105547/66ac520a-8f8f-11e3-979c-8529edea5113.png)
and wrong:…
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The allele tab on the disease page has OMIM icons that can be hard to read. Furthermore, the OMIM icons link to the Neurolex entry about OMIM as a whole. We should add a text label and link to the OM…
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For example, see diseases on this page:
http://monarchinitiative.org/phenotype/HP_0100257
Which has an entry that states "Moved to 615465"
clicking on the link takes you here
http://monarchinitiative.…
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Analyze /phenotypes should include the model-view grid that is shown on the disease page.
should this be on a different tab on the same page , or should we reithink the analyze/phenotypes page more …
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Stick is non-uniformly escaping html, and causing all sorts of problems with genotypes and alleles during display. This will need to get tracked down and fixed somehow.
things that end up escaped …