SACGF / SACGF/variantgrid

Phenotype aliases / overrides in database

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Ontology
Dominant language
Python
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Description

There are 200 lines of HPO/OMIM alias code in phenotype_matching.py - perhaps move these into the DB so that other people can easily add aliases etc.

Maybe even allow uploading a spreadsheet of aliases - that way can fix pheno matches much more quickly w/o code changes etc

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May want to add a view phenotypes page, and be able to search on them. Can see gene list, show gene lists, patients, classifications, what's aliased to it etc.

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