{
  "id": 16665,
  "label": "benign neonatal seizures",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0016027",
  "properties": {
    "xrefs": [
      "DOID:14264",
      "DOID:14777",
      "GARD:0001519",
      "MEDGEN:65082",
      "MedDRA:10067866",
      "NCIT:C117307",
      "OMIMPS:121200",
      "Orphanet:1949",
      "SCTID:279953009",
      "SCTID:38281008",
      "UMLS:C0220669"
    ],
    "synonyms": [
      "BFNS",
      "benign familal neonatal seizures",
      "benign familial convulsion",
      "benign familial convulsions",
      "benign familial neonatal convulsions",
      "benign familial neonatal epilepsy",
      "benign familial neonatal seizures",
      "seizures, benign familial neonatal"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare genetic epilepsy syndrome characterized by the occurrence of afebrile seizures in otherwise healthy newborns with onset in the first few days of life."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "id": 19723,
      "label": "neonatal epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019435",
          "Orphanet:98257"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome that has an onset during the neonatal stage of life."
      },
      "child_count": 6,
      "reference_id": "MONDO:0020070"
    },
    {
      "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": [
    {
      "id": 8758,
      "label": "seizures, benign familial neonatal, 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16665
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0009765",
          "MEDGEN:460425",
          "MESH:C567743",
          "OMIM:121200",
          "UMLS:C3149074"
        ],
        "synonyms": [
          "myokymia",
          "KCNQ2 benign neonatal seizures",
          "benign neonatal seizures caused by mutation in KCNQ2",
          "seizures, benign familial neonatal, 1",
          "seizures, benign familial neonatal, type 1",
          "seizures, benign neonatal, 1",
          "BFNS1",
          "epilepsy, benign neonatal, 1, and/or myokymia",
          "seizures, benign familial neonatal, 1, and/or myokymia"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ2 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007365"
    },
    {
      "id": 8759,
      "label": "seizures, benign familial neonatal, 2",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16665
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015054",
          "MEDGEN:377707",
          "OMIM:121201",
          "UMLS:C1852581"
        ],
        "synonyms": [
          "KCNQ3 benign neonatal seizures",
          "benign neonatal seizures caused by mutation in KCNQ3",
          "seizures, benign familial neonatal, 2",
          "seizures, benign familial neonatal, type 2",
          "seizures, benign neonatal, 2",
          "BFNS2",
          "convulsions, benign familial neonatal, 2"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any benign neonatal seizures in which the cause of the disease is a mutation in the KCNQ3 gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0007366"
    },
    {
      "id": 11215,
      "label": "seizures, benign familial neonatal, autosomal recessive",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16665
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015234",
          "MEDGEN:338640",
          "MESH:C564823",
          "OMIM:269720",
          "UMLS:C1849250"
        ],
        "synonyms": [
          "seizures, benign familial neonatal, autosomal recessive",
          "Bfns, autosomal recessive",
          "autosomal dominant form of benign neonatal seizures",
          "convulsions benign familial neonatal dominant form",
          "convulsions, benign familial neonatal, autosomal recessive",
          "epilepsy, benign familial neonatal, autosomal recessive"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0010021"
    },
    {
      "id": 13061,
      "label": "seizures, benign familial neonatal, 3",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16665
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0015427",
          "MEDGEN:334063",
          "MESH:C564274",
          "OMIM:608217",
          "UMLS:C1842382"
        ],
        "synonyms": [
          "BFNS3",
          "seizures, benign familial neonatal, 3",
          "convulsions, benign familial neonatal, 3"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0011990"
    }
  ],
  "roots": [
    {
      "id": 19723,
      "label": "neonatal epilepsy syndrome"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}