{
  "id": 18280,
  "label": "brain dopamine-serotonin vesicular transport disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018130",
  "properties": {
    "xrefs": [
      "DOID:0070490",
      "GARD:0013594",
      "MEDGEN:929215",
      "OMIM:618049",
      "Orphanet:352649",
      "SCTID:717942003",
      "UMLS:C4303546"
    ],
    "synonyms": [
      "PKDYS2",
      "parkinsonism-dystonia, infantile, 2"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An infantile-onset neurometabolic disease characterized by dystonia, parkinsonism, nonambulation, autonomic dysfunction, developmental delay and mood disturbances."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 14186,
      "label": "parkinsonism-dystonia, infantile",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        19719,
        20335
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010484",
          "MEDGEN:413468",
          "MESH:C567730",
          "OMIMPS:613135",
          "Orphanet:238455",
          "UMLS:C2751067"
        ],
        "synonyms": [
          "IPD",
          "PARKINSONISM-dystonia, infantile",
          "PKDYS",
          "Parkinsonism-dystonia infantile",
          "dopamine transporter deficiency syndrome",
          "infantile Parkinsonism-dystonia",
          "parkinsonism-dystonia, infantile"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Infantile dystonia-parkinsonism (IPD) is an extremely rare inherited neurological syndrome that presents in early infancy with hypokinetic parkinsonism and dystonia and that can be fatal."
      },
      "child_count": 9,
      "reference_id": "MONDO:0013150"
    },
    {
      "id": 19086,
      "label": "inborn disorder of neurotransmitter metabolism and transport",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19112
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018950",
          "MEDGEN:1842206",
          "Orphanet:79169",
          "UMLS:C5681289"
        ],
        "synonyms": [
          "disorder of neurotransmitter metabolism and transport"
        ]
      },
      "child_count": 4,
      "reference_id": "MONDO:0019219"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 14186,
      "label": "parkinsonism-dystonia, infantile"
    },
    {
      "id": 19086,
      "label": "inborn disorder of neurotransmitter metabolism and transport"
    }
  ]
}