{
  "id": 3056,
  "label": "akinetopsia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0000660",
  "properties": {
    "xrefs": [
      "DOID:0060130",
      "GARD:0022816"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "An agnosia that is a loss of motion perception."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 6812,
      "label": "mental disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4172,
        7209
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0000677",
          "ICD9:290-299",
          "ICD9:298.8",
          "ICD9:V11.9",
          "MEDGEN:14047",
          "SCTID:74732009",
          "UMLS:C0004936",
          "birnlex:12669"
        ],
        "synonyms": [
          "disorder of mental process",
          "mental or behavioral disorder",
          "mental or behavioural disorder",
          "mental process disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease that has its basis in the disruption of mental process."
      },
      "child_count": 28,
      "reference_id": "MONDO:0005084"
    },
    {
      "id": 7275,
      "label": "agnosia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        21402
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:4090",
          "EFO:0007136",
          "GARD:0027722",
          "ICD10CM:R48.1",
          "MEDGEN:174",
          "MESH:D000377",
          "NCIT:C84542",
          "SCTID:68345001",
          "UMLS:C0001816",
          "icd11.foundation:1315065296"
        ],
        "synonyms": [
          "agnosia",
          "Monomodal visual amnesia",
          "primary visual agnosia",
          "visual amnesia",
          "dyspraxia (finding)",
          "dyspraxia syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare disorder characterized by the lack of ability to recognize individuals, objects, shapes, sounds, or smells. There is no loss of memory. It is caused by neurological damage in the brain, specifically in the occipital or parietal lobes."
      },
      "child_count": 20,
      "reference_id": "MONDO:0005638"
    },
    {
      "id": 18957,
      "label": "neuromuscular disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:440",
          "EFO:1001902",
          "ICD9:358",
          "ICD9:358.9",
          "MEDGEN:10323",
          "MESH:D009468",
          "MedDRA:10029323",
          "NANDO:1100001",
          "NANDO:2100214",
          "Orphanet:68381",
          "UMLS:C0027868"
        ],
        "synonyms": [
          "nerve and muscle disorder",
          "neuromuscular disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any disease that impairs the functioning of the muscles, either directly, being pathologies of the voluntary muscle, or indirectly, being pathologies of nerves or neuromuscular junctions"
      },
      "child_count": 8,
      "reference_id": "MONDO:0019056"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 6812,
      "label": "mental disorder"
    },
    {
      "id": 7275,
      "label": "agnosia"
    },
    {
      "id": 18957,
      "label": "neuromuscular disease"
    }
  ]
}