{
  "id": 15939,
  "label": "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0014960",
  "properties": {
    "xrefs": [
      "EFO:0009158",
      "GARD:0025040",
      "OMIMPS:617186"
    ],
    "synonyms": [
      "PEBEL",
      "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy",
      "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy; PEBEL",
      "encephalopathy, progressive, early-onset, with brain oedema and/or leukoencephalopathy; PEBEL"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7208,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020280",
          "MEDGEN:1825988",
          "MESH:D020271",
          "NCIT:C97073",
          "Orphanet:183500",
          "UMLS:C5680568"
        ],
        "synonyms": [
          "genetic neurodegenerative disease",
          "hereditary neurodegenerative disease",
          "hereditary neurodegenerative disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An inherited disorder characterized by progressive degeneration and atrophy of the nervous system."
      },
      "child_count": 164,
      "reference_id": "MONDO:0024237"
    },
    {
      "id": 23939,
      "label": "Mendelian encephalopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "definition": "An instance of encephalopathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 19,
      "reference_id": "MONDO:0100198"
    }
  ],
  "children": [
    {
      "id": 20182,
      "label": "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        15939
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017991",
          "MEDGEN:934642",
          "OMIM:617186",
          "Orphanet:555407",
          "UMLS:C4310675"
        ],
        "synonyms": [
          "encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy",
          "encephalopathy, progressive, early-onset, with brain oedema and/or leukoencephalopathy",
          "NAD(P)HX epimerase deficiency",
          "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 1",
          "PEBEL1"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0020781"
    },
    {
      "id": 22772,
      "label": "NAD(P)HX dehydratase deficiency",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        7611,
        15939,
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0017990",
          "MEDGEN:1681210",
          "OMIM:618321",
          "Orphanet:555402",
          "UMLS:C5193026"
        ],
        "synonyms": [
          "ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 2",
          "PEBEL2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0034121"
    }
  ],
  "roots": [
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    },
    {
      "id": 23939,
      "label": "Mendelian encephalopathy"
    }
  ]
}