Merge pull request #303 from matentzn/phenotype-counts

Update 13K phenotype count to 18K on two pages

src/app/static/about/about.component.html

@@ -19,7 +19,7 @@ <h3 class="sub-title">Who we are!</h3>
         (<a href="https://www.ncbi.nlm.nih.gov/pubmed/27899602" target="__blank">K&ouml;hler et al, 2017</a>).
       </p>
       <p>
-        The HPO currently contains over 13,000 terms arranged in a directed acyclic graph and are connected by is-a
+        The HPO currently contains over 18,000 terms arranged in a directed acyclic graph and are connected by is-a
         (subclass-of) edges, such that a term represents
         a more specific or limited instance of its parent term(s). All relationships in the HPO are is-a relationships,
         i.e. simple class-subclass relationships. For instance, <a routerLink="/browse/term/HP:0000517"><em>Abnormal lens

src/app/static/home/home.component.html

@@ -16,7 +16,7 @@ <h2>The Human Phenotype Ontology</h2>
       <p>The Human Phenotype Ontology (HPO) provides a standardized vocabulary of phenotypic abnormalities encountered
         in human disease. Each term in the HPO describes a phenotypic abnormality, such as
         <a routerLink="/browse/term/HP:0001631">Atrial septal defect</a>. The HPO is currently being developed using
-        the medical literature, Orphanet, DECIPHER, and OMIM. HPO currently contains over 13,000 terms and over
+        the medical literature, Orphanet, DECIPHER, and OMIM. HPO currently contains over 18,000 terms and over
         156,000 annotations to hereditary diseases. The HPO project and others have developed software for
         phenotype-driven differential diagnostics, genomic diagnostics, and translational research. The HPO is a
         flagship product of the <a href="https://monarchinitiative.org/" target="__blank">Monarch Initiative</a>,