wzkariampuzha commited on
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eddce31
1 Parent(s): cde5ff7

Update app.py

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Files changed (1) hide show
  1. app.py +1 -1
app.py CHANGED
@@ -73,7 +73,7 @@ with st.spinner('Loading Epidemiology Models and Dependencies...'):
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  st.success('All Models and Dependencies Loaded!')
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  disease_or_gard_id = st.text_input("Input a rare disease term or GARD ID.")
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- st.markdown("Examples of rare diseases include Fellman syndrome, Classic Homocystinuria, phenylketonuria, and GARD:0009941. A full list of rare diseases tracked by GARD can be found [here](https://rarediseases.info.nih.gov/diseases/browse-by-first-letter)")
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  if disease_or_gard_id:
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  df = extract_abs.streamlit_extraction(disease_or_gard_id, max_results, filtering,
 
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  st.success('All Models and Dependencies Loaded!')
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  disease_or_gard_id = st.text_input("Input a rare disease term or GARD ID.")
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+ 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), [**phenylketonuria**](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 GARD can be found [here](https://rarediseases.info.nih.gov/diseases/browse-by-first-letter).")
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  if disease_or_gard_id:
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  df = extract_abs.streamlit_extraction(disease_or_gard_id, max_results, filtering,