Update app.py

app.py

@@ -105,13 +105,11 @@ with st.spinner('Loading Epidemiology Models and Dependencies...'):
     classify_model_vars, NER_pipeline, entity_classes, GARD_dict, max_length = load_models_experimental()
 loaded = st.success('All Models and Dependencies Loaded!')
 
-disease_or_gard_id = st.text_input("Input a rare disease term or GARD ID.")
+disease_or_gard_id = st.text_input("Input a rare disease term or NIH GARD ID.")
 
 loaded.empty()
 
-st.markdown("Examples of rare diseases include [**Fellman syndrome**](https://rarediseases.info.nih.gov/diseases/1/gracile-syndrome), [**Classic Homocystinuria**](https://rarediseases.info.nih.gov/diseases/6667/classic-homocystinuria), [**7383**](https://rarediseases.info.nih.gov/diseases/7383/phenylketonuria), and [**GARD:0009941**](https://rarediseases.info.nih.gov/diseases/9941/fshmd1a).")
-
-st.markdown("A full list of rare diseases tracked by GARD can be found [here](https://rarediseases.info.nih.gov/diseases/browse-by-first-letter).")
+st.markdown("Examples of rare diseases include [**Fellman syndrome**](https://rarediseases.info.nih.gov/diseases/1/gracile-syndrome), [**Classic Homocystinuria**](https://rarediseases.info.nih.gov/diseases/6667/classic-homocystinuria), [**7383**](https://rarediseases.info.nih.gov/diseases/7383/phenylketonuria), and [**GARD:0009941**](https://rarediseases.info.nih.gov/diseases/9941/fshmd1a). A full list of rare diseases tracked by the NIH Genetic and Rare Diseases Information Center (GARD) can be found [here](https://rarediseases.info.nih.gov/diseases/browse-by-first-letter).")
 
 if disease_or_gard_id:
     df, sankey_data = extract_abs.streamlit_extraction(disease_or_gard_id, max_results, filtering,