Identifying facial phenotypes of genetic disorders using deep learning.

Journal: Nature medicine
Published Date:

Abstract

Syndromic genetic conditions, in aggregate, affect 8% of the population. Many syndromes have recognizable facial features that are highly informative to clinical geneticists. Recent studies show that facial analysis technologies measured up to the capabilities of expert clinicians in syndrome identification. However, these technologies identified only a few disease phenotypes, limiting their role in clinical settings, where hundreds of diagnoses must be considered. Here we present a facial image analysis framework, DeepGestalt, using computer vision and deep-learning algorithms, that quantifies similarities to hundreds of syndromes. DeepGestalt outperformed clinicians in three initial experiments, two with the goal of distinguishing subjects with a target syndrome from other syndromes, and one of separating different genetic subtypes in Noonan syndrome. On the final experiment reflecting a real clinical setting problem, DeepGestalt achieved 91% top-10 accuracy in identifying the correct syndrome on 502 different images. The model was trained on a dataset of over 17,000 images representing more than 200 syndromes, curated through a community-driven phenotyping platform. DeepGestalt potentially adds considerable value to phenotypic evaluations in clinical genetics, genetic testing, research and precision medicine.

Authors

  • Yaron Gurovich
    FDNA Inc., Boston, MA, USA. yaron@fdna.com.
  • Yair Hanani
    FDNA Inc., Boston, MA, USA.
  • Omri Bar
    FDNA Inc., Boston, MA, USA.
  • Guy Nadav
    Functional Brain Center, The Wohl Institute for Advanced Imaging, Tel Aviv Sourasky Medical Center, 6 Weizman St., 64239, Tel Aviv, Israel.
  • Nicole Fleischer
    FDNA Inc., Boston, MA, USA.
  • Dekel Gelbman
    FDNA Inc., Boston, MA, USA.
  • Lina Basel-Salmon
    Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Peter M Krawitz
    Institute for Genomic Statistic and Bioinformatics, University Hospital Bonn, Rheinische-Friedrich-Wilhelms University, Bonn, Germany.
  • Susanne B Kamphausen
    Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
  • Martin Zenker
    Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
  • Lynne M Bird
    Department of Pediatrics, University of California San Diego, San Diego, CA, USA.
  • Karen W Gripp
    Division of Medical Genetics, A. I. du Pont Hospital for Children/Nemours, Wilmington, DE, USA.