{
  "id": 14148,
  "label": "neurodegenerative syndrome due to cerebral folate transport deficiency",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0013110",
  "properties": {
    "xrefs": [
      "DOID:0050719",
      "GARD:0010594",
      "ICD9:266.2",
      "MEDGEN:442763",
      "MESH:C567791",
      "OMIM:613068",
      "Orphanet:217382",
      "SCTID:711403001",
      "UMLS:C2751584",
      "icd11.foundation:1158040363"
    ],
    "synonyms": [
      "neurodegenerative syndrome due to cerebral folate transport deficiency",
      "cerebral folate deficiency syndrome",
      "cerebral folate transport deficiency",
      "neurodegeneration due to cerebral folate TRANSPORT deficiency"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7182,
      "label": "inborn vitamin metabolic disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18954,
        21331
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050718",
          "EFO:0005596",
          "GARD:0024204"
        ],
        "synonyms": [
          "inborn error of vitamin metabolic process",
          "inborn vitamin metabolic process disorder",
          "rare inborn error of vitamin metabolic process",
          "vitamin metabolic disorder"
        ],
        "definition": "An inherited metabolic disease that is has its basis in the disruption of vitamin metabolic process."
      },
      "child_count": 10,
      "reference_id": "MONDO:0005528"
    },
    {
      "id": 17632,
      "label": "disorder of folate metabolism and transport",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        17984
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021131",
          "MEDGEN:1842423",
          "Orphanet:285657",
          "UMLS:C5681010",
          "icd11.foundation:2081529009"
        ]
      },
      "child_count": 7,
      "reference_id": "MONDO:0017313"
    },
    {
      "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"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 7182,
      "label": "inborn vitamin metabolic disorder"
    },
    {
      "id": 17632,
      "label": "disorder of folate metabolism and transport"
    },
    {
      "id": 21292,
      "label": "inherited neurodegenerative disorder"
    }
  ]
}