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Update 13K phenotype count to 18K on two pages #303

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2 changes: 1 addition & 1 deletion src/app/static/about/about.component.html
Original file line number Diff line number Diff line change
Expand Up @@ -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
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2 changes: 1 addition & 1 deletion src/app/static/home/home.component.html
Original file line number Diff line number Diff line change
Expand Up @@ -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>,
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