a26e6bfa1bc310a809138e7c39bdcf5ea29a79ef
lrnassar
  Tue Jul 16 17:13:07 2024 -0700
Nesting OMIM into a single superTrack, refs #25682

diff --git src/hg/makeDb/trackDb/human/omimContainer.html src/hg/makeDb/trackDb/human/omimContainer.html
new file mode 100644
index 0000000..f60040f
--- /dev/null
+++ src/hg/makeDb/trackDb/human/omimContainer.html
@@ -0,0 +1,24 @@
+<p>
+OMIM is a compendium of human genes and genetic phenotypes. The full-text, 
+referenced overviews in OMIM contain information on all known Mendelian 
+disorders and over 12,000 genes. OMIM is authored and edited at the McKusick-Nathans 
+Institute of Genetic Medicine, Johns Hopkins University School of Medicine, under 
+the direction of Dr. Ada Hamosh. This database was initiated in the early 1960s 
+by Dr. Victor A. McKusick as a catalog of Mendelian traits and disorders, 
+entitled Mendelian Inheritance in Man (MIM).</p>
+
+<p>
+The OMIM data are separated into three separate tracks:<br><br> 
+
+<b>OMIM Alellic Variant Phenotypes (OMIM Alleles)</b> - Variants in the OMIM 
+database that have associated dbSNP identifiers.<br><br>
+
+<b>OMIM Gene Phenotypes (OMIM Genes)</b> - The genomic positions of gene 
+entries in the OMIM database. The coloring indicates the associated OMIM phenotype map key.<br><br>
+
+<b>OMIM Cytogenetic Loci Phenotypes: Gene Unknown (OMIM Cyto Loci)</b> - Regions 
+known to be associated with a phenotype, but for which no specific gene is known 
+to be causative. This track also includes known multi-gene syndromes.<br><br>
+
+Clicking into the individual tracks provides additional information including display conventions.
+</p>