{
  "id": 22479,
  "label": "developmental and epileptic encephalopathy, 80",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0032822",
  "properties": {
    "xrefs": [
      "DOID:0112216",
      "GARD:0025754",
      "MEDGEN:1684779",
      "OMIM:618580",
      "UMLS:C5231418"
    ],
    "synonyms": [
      "DEE80",
      "EIEE80",
      "EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 80",
      "developmental and epileptic encephalopathy 80",
      "epileptic encephalopathy, early infantile, 80",
      "Glycosylphosphatidylinositol Biosynthesis Defect 20"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3146",
          "GARD:0021314",
          "ICD9:272.8",
          "ICD9:272.9",
          "MEDGEN:57587",
          "MedDRA:10061227",
          "NCIT:C97092",
          "Orphanet:309005",
          "SCTID:267431006",
          "SCTID:402788005",
          "UMLS:C0154251"
        ],
        "synonyms": [
          "disorder of lipid metabolism",
          "dyslipidaemia",
          "dyslipidemia",
          "lipid metabolism disorder",
          "fatty acid metabolism disorder"
        ],
        "definition": "An inherited metabolic disorder caused by an enzyme deficiency, resulting in an inability to oxidize fatty acids for energy production."
      },
      "child_count": 29,
      "reference_id": "MONDO:0002525"
    },
    {
      "id": 21353,
      "label": "disorder of GPI anchor biosynthesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6795,
        21354
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "GPI anchor biosynthetic process disease",
          "GPIBD",
          "disorder of GPI anchor biosynthetic process",
          "glycosylphosphatidylinositol biosynthesis defect"
        ],
        "definition": "A disease that has its basis in the disruption of GPI anchor biosynthetic process."
      },
      "child_count": 22,
      "reference_id": "MONDO:0024321"
    },
    {
      "id": 23814,
      "label": "genetic developmental and epileptic encephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        24226,
        24340
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112202",
          "GARD:0009255",
          "ICD9:345.10",
          "NANDO:1200593",
          "NCIT:C122814",
          "OMIMPS:308350"
        ],
        "synonyms": [
          "developmental and epileptic encephalopathy",
          "hereditary developmental and epileptic encephalopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A complex neurodevelopmental disorder characterized by a range of developmental delays and epileptic encephalopathy phenotypes. Seizure onset is variable and intellectual disability is variable in presence and severity."
      },
      "child_count": 210,
      "reference_id": "MONDO:0100062"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4594,
      "label": "inherited lipid metabolism disorder"
    },
    {
      "id": 21353,
      "label": "disorder of GPI anchor biosynthesis"
    },
    {
      "id": 23814,
      "label": "genetic developmental and epileptic encephalopathy"
    }
  ]
}