4fde51d367a488060e18e0e19d18a2594915ae76
abenetpa
  Thu Jul 2 14:59:11 2020 -0700
corrected typo in description refs #25815

diff --git src/hg/makeDb/trackDb/human/omimGene2.html src/hg/makeDb/trackDb/human/omimGene2.html
index 0e64c48..d87b41d 100644
--- src/hg/makeDb/trackDb/human/omimGene2.html
+++ src/hg/makeDb/trackDb/human/omimGene2.html
@@ -98,31 +98,31 @@
     <td>Y-Linked</td>
     <td>YL</td>
   </tr>
 </table>
 </P>
 <P>
 <b>Brackets, "[ ]"</b>, before the phenotype name indicate "nondiseases," mainly genetic variations that
 lead to apparently abnormal laboratory test values (e.g., dysalbuminemic euthyroidal 
 hyperthyroxinemia).
 </P>
 <P>
 <b>Braces, "{ }"</b>, indicate mutations that contribute to susceptibility to multifactorial disorders
 (e.g., diabetes, asthma) or to susceptibility to infection (e.g., malaria).
 </P>
 <P>
-A <b>question mark, "?"</b>, indicates that the relationship between the phenotype and gene is provisional.
+<b>Question marks, "?"</b>, indicate that the relationship between the phenotype and gene is provisional.
 More details about this relationship are provided in the comment field of the map and in the gene
 and phenotype OMIM entries.
 </P>
 
 <H2>Methods</H2>
 <P>
 The mappings displayed in this track are based on OMIM gene entries, their Entrez Gene IDs, and
 the corresponding RefSeq Gene locations:
 <UL>
 <LI>The data file <TT>genemap.txt</TT> from OMIM was loaded into the MySQL table <TT>omimGeneMap</TT>.
 <LI>The data file <TT>mim2gene.txt</TT> from OMIM was processed and loaded into the MySQL table <TT>omim2gene</TT>.
 <LI>Entries in <TT>genemap.txt</TT> having disorder info were parsed and loaded into the 
 <TT>omimPhenotype</TT> table.
 <LI>For each OMIM gene in the <TT>omim2gene</TT> table, the
 <A HREF="https://www.ncbi.nlm.nih.gov/gene" TARGET=_blank>Entrez Gene ID</A> was used to get the