{
  "id": 5178,
  "label": "prosopagnosia",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0003227",
  "properties": {
    "xrefs": [
      "DOID:4970",
      "GARD:0027636",
      "HP:0010528",
      "MEDGEN:65884",
      "MESH:D020238",
      "NCIT:C85031",
      "UMLS:C0234512",
      "icd11.foundation:858616900"
    ],
    "synonyms": [
      "face blindness",
      "prosopagnosia",
      "prosopagnosia (disease)"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Impaired ability to recognize other human faces in the absence of a vision disorder. It may be a congenital disorder or the result of brain injury."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "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"
    }
  ],
  "children": [
    {
      "id": 13533,
      "label": "prosopagnosia, hereditary",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        5178,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0010035",
          "MEDGEN:419809",
          "MESH:C537242",
          "OMIM:610382",
          "UMLS:C2931455"
        ],
        "synonyms": [
          "hereditary prosopagnosia (disease)",
          "prosopagnosia, hereditary",
          "congenital prosopagnosia",
          "developmental prosopagnosia",
          "face blindness",
          "hereditary prosopagnosia",
          "prosopagnosia, congenital",
          "prosopagnosia, developmental"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An instance of prosopagnosia (disease) that is caused by an inherited modification of the individual's genome."
      },
      "child_count": 0,
      "reference_id": "MONDO:0012484"
    }
  ],
  "roots": [
    {
      "id": 7275,
      "label": "agnosia"
    }
  ]
}