{
  "diseaseName": "Genetic Diseases, Inborn",
  "diseaseId": "DOID:630",
  "diseaseOntology": "DOID",
  "diseaseDescription": null,
  "associations": [
    {
      "associationType": "CTD",
      "associationDescription": "Gene-Disease associations with direct evidence from the Comparative Toxicogenomics Database.",
      "associationSource": null,
      "tcrdProteinId": 5290,
      "uniprotId": "P11473",
      "tcrdGeneSymbol": "VDR"
    }
  ]
}