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. 2016 Nov 24;45(Database issue):D877–D887. doi: 10.1093/nar/gkw1012

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© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

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Figure 1. — Overlaps among disease sources. (A) Venn diagram for the four major MalaCards name sources, according to MalaCards mapping. (B) A symmetric matrix showing the number of overlapping diseases between all pairs of primary name sources according to MalaCards mapping. Shading (as per color bar) and numerals represent degree of overlap in disease counts. Source abbreviations: DO– Disease Ontology, GR- Gene Reviews, NIH RD– NIH Rare Diseases, GT- GeneTests, GHR- Genetic Home Reference, NINDS– National Institute of Neurological Disorders and Stroke.