{
  "id": 13533,
  "label": "prosopagnosia, hereditary",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012484",
  "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."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 5178,
      "label": "prosopagnosia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7275
      ],
      "type_id": 0,
      "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."
      },
      "child_count": 1,
      "reference_id": "MONDO:0003227"
    },
    {
      "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": 5178,
      "label": "prosopagnosia"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}