{
  "id": 21414,
  "label": "neurodegeneration with brain iron accumulation 2A",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0024457",
  "properties": {
    "xrefs": [
      "DOID:0110735",
      "GARD:0003957",
      "ICD9:330.8",
      "MEDGEN:82852",
      "MESH:C536071",
      "NANDO:1200537",
      "NCIT:C84927",
      "OMIM:256600",
      "Orphanet:35069",
      "SCTID:52713000",
      "UMLS:C0270724"
    ],
    "synonyms": [
      "Seitelberger disease",
      "INAD",
      "NBIA2A",
      "NBIA2a",
      "PLAN",
      "inaD",
      "infantile neuroaxonal dystrophy",
      "neurodegeneration with brain iron accumulation 2A",
      "neurodegeneration with brain iron accumulation type 2A",
      "neurodegeneration with brain iron accumulation type 2a",
      "neurodegeneration, PLA2G6-associated",
      "neurodegeneration, Pla2G6-associated",
      "neurodegeneration, Pla2g6-associated",
      "phospholipase A2-associated neurodegeneration",
      "Hunter Carpenter Macdonald syndrome",
      "Hunter-Carpenter-McDonald syndrome",
      "INAD1",
      "KARAK syndrome, included",
      "infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy",
      "neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene",
      "neuroaxonal dystrophy, infantile"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 18173,
      "label": "PLA2G6-associated neurodegeneration",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18404
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012567",
          "NORD:1302",
          "Orphanet:329303"
        ],
        "synonyms": [
          "PLA2G6 neurodegeneration with brain iron accumulation",
          "PLAN",
          "neurodegeneration with brain iron accumulation caused by mutation in PLA2G6"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any neurodegeneration with brain iron accumulation in which the cause of the disease is a mutation in the PLA2G6 gene."
      },
      "child_count": 3,
      "reference_id": "MONDO:0017998"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6950,
        24271
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010711",
          "MEDGEN:1825937",
          "Orphanet:98497",
          "UMLS:C5681733"
        ],
        "synonyms": [
          "genetic peripheral neuropathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of peripheral neuropathy that is caused by an inherited genomic modification in an individual."
      },
      "child_count": 130,
      "reference_id": "MONDO:0020127"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 18173,
      "label": "PLA2G6-associated neurodegeneration"
    },
    {
      "id": 19748,
      "label": "hereditary peripheral neuropathy"
    }
  ]
}