{
  "id": 14244,
  "label": "cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013208",
  "properties": {
    "xrefs": [
      "DOID:0080536",
      "GARD:0010706",
      "ICD9:277.89",
      "MEDGEN:412958",
      "MESH:C548016",
      "OMIM:613280",
      "Orphanet:309854",
      "SCTID:702377007",
      "UMLS:C2750442"
    ],
    "synonyms": [
      "cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome",
      "HMDPC",
      "HMNDYT1",
      "hypermanganesemia with dystonia 1",
      "hypermanganesemia with dystonia polycythemia and cirrhosis",
      "hypermanganesemia with dystonia, polycythemia, and cirrhosis"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2773,
      "label": "hypermanganesemia with dystonia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080535",
          "GARD:0022727",
          "MEDGEN:1632594",
          "OMIMPS:613280",
          "SCTID:768553002",
          "UMLS:C4708509"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0000214"
    },
    {
      "id": 17991,
      "label": "disorder of manganese transport",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17986
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021358",
          "MEDGEN:1843191",
          "Orphanet:309851",
          "UMLS:C5681032"
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0017766"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5849
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080855",
          "MEDGEN:66079",
          "MESH:D020734",
          "UMLS:C0242422"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA."
      },
      "child_count": 21,
      "reference_id": "MONDO:0021095"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6799
      ],
      "type_id": 0,
      "properties": {
        "synonyms": [
          "neurogenetic disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A heterogeneous group of genetic conditions with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology characterized by abnormalities in the brain, spinal cord, nerves, or muscles."
      },
      "child_count": 528,
      "reference_id": "MONDO:0100545"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2773,
      "label": "hypermanganesemia with dystonia"
    },
    {
      "id": 17991,
      "label": "disorder of manganese transport"
    },
    {
      "id": 20335,
      "label": "parkinsonian disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}