{
  "id": 15401,
  "label": "ataxia-telangiectasia-like disorder 2",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014399",
  "properties": {
    "xrefs": [
      "DOID:0081385",
      "GARD:0017736",
      "MEDGEN:863113",
      "OMIM:615919",
      "Orphanet:438134",
      "UMLS:C4014676"
    ],
    "synonyms": [
      "ataxia-telangiectasia-like disorder 2",
      "ataxia-telangiectasia-like disorder type 2",
      "ATLD2",
      "PCNA-related progressive neurodegenerative photosensitivity syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 12561,
      "label": "ataxia-telangiectasia-like disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21292
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024799",
          "ICD9:334.8",
          "MEDGEN:348929",
          "MESH:C565779",
          "OMIMPS:604391",
          "SCTID:700058006",
          "UMLS:C1858391",
          "icd11.foundation:242329289"
        ],
        "synonyms": [
          "ATLD",
          "ataxia - telangiectasia-like disorder",
          "ataxia-telangiectasia-like disorder type 1",
          "ATLD1",
          "ataxia-telangiectasia-like disorder 1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An autosomal recessive condition caused by mutation(s) in the MRE11A gene, encoding double-strand break repair protein MRE11. It is characterized by progressive cerebellar degeneration resulting in ataxia and oculomotor apraxia."
      },
      "child_count": 3,
      "reference_id": "MONDO:0011457"
    },
    {
      "id": 20416,
      "label": "DNA repair disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0008499",
          "GARD:0025299",
          "MEDGEN:82774",
          "MESH:D049914",
          "NCIT:C7757",
          "UMLS:C0268134"
        ],
        "synonyms": [
          "DNA repair disorder",
          "deficiency of DNA repair",
          "disorder of DNA repair",
          "DNA Repairs, deficient",
          "DNA repair deficiency",
          "DNA repair deficiency disorders",
          "DNA repair, deficient",
          "DNA repair-deficiencies",
          "DNA repair-deficiency",
          "DNA repair-deficiency disorder",
          "Repairs, deficient DNA",
          "chromosome instability syndrome",
          "chromosome instability syndromes",
          "deficient DNA Repairs",
          "deficient DNA repair",
          "disorder, DNA repair-deficiency",
          "disorders, DNA repair-deficiency",
          "repair, deficient DNA",
          "syndrome, chromosome instability",
          "syndromes, chromosome instability"
        ],
        "definition": "A disease that has its basis in the disruption of DNA repair."
      },
      "child_count": 16,
      "reference_id": "MONDO:0021190"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 12561,
      "label": "ataxia-telangiectasia-like disorder"
    },
    {
      "id": 20416,
      "label": "DNA repair disease"
    }
  ]
}