Here is a plan for Mondo parsing:
https://github.com/monarch-initiative/phenol/issues/23
Prior to this, I would split the phenotype and the disease data into two separate tabs
I would show the OMIM and Orpha annotations that correspond to any given Mondo term.
Here is a plan for Mondo parsing: https://github.com/monarch-initiative/phenol/issues/23 Prior to this, I would split the phenotype and the disease data into two separate tabs I would show the OMIM and Orpha annotations that correspond to any given Mondo term.