AnDDI-Clic

Developed by the AnDDI-Rares network, the AnDDI-Clic illustrations facilitate exchanges between healthcare professionals and families, avoiding the use of medical terms by presenting concepts with images. 

Example from the developmental anomalies board

The illustrations are available in English and blank PPT versions. Feel free to add text in your own language. 

There are 11 sections covering different asepcts of human and clinical genetics: 

  1. General (English/Blank)
  2. Patterns of inheritance (English/Blank)
  3. Sampling (English/Blank)
  4. Prenatal and preimplantation diagnoses (English/Blank)
  5. Genetic diagnostic technologies (English/Blank)
  6. Genetic variations (English/Blank)
  7. Genomic research strategies (English/Blank)
  8. Developmental anomalies (English/Blank)
  9. Personalised medicine and therapy (English/Blank)
  10. Organisation of rare diseases (English/Blank)
  11. Others (English/Blank)

AnDDI-Rares is the French national rare disease network dedicated to diseases with developmental abnormalities, with or without intellectual disability

English versions

1. General – English
2. Patterns of inheritance – English
3. Samplings – English
4. Prenatal and preimplantation diagnoses
5. Genetic Diagnosis Technologies
6. Genetic variations
7. Genetic research strategies
8. Developmental anomalies
9. Personalised medicine & therapy
10. Organisations of rare diseases
11. Others
Full powerpoint

Blank versions

1. General – Blank
2. Patterns of inheritance – Blank
3. Samplings – Blank
4. Prenatal and preimplantation diagnoses – Blank
5. Genetic Diagnosis Technologies – Blank
6. Genetic variations – Blank
7. Genetic research strategies – Blank
8. Developmental anomalies – Blank
9. Personalised medicine & therapy – Blank
10. Organisations of rare diseases – Blank
11. Others – Blank