Fig. 3From: Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case seriesDiagnostic rates by phenotype for ES (n = 76 cases). Human phenotype ontology terms generated from clinical presentation. Diagnostic rates are shown (%) together with number of cases for a given phenotype where a molecular diagnosis was made (filled boxes) or no diagnosis made (white boxes)Back to article page