{
  "id": 16428,
  "label": "benign partial infantile seizures",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0015642",
  "properties": {
    "xrefs": [
      "GARD:0020076",
      "MEDGEN:1842641",
      "Orphanet:166311",
      "UMLS:C5680426"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 5,
  "parents": [
    {
      "id": 19724,
      "label": "infantile epilepsy syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16436
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019436",
          "Orphanet:98258"
        ],
        "synonyms": [
          "epilepsy syndrome of infancy",
          "infantile epilepsy syndrome",
          "infantile onset epilepsy syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An epilepsy syndrome that occurs between 28 days to one year of life."
      },
      "child_count": 9,
      "reference_id": "MONDO:0020071"
    }
  ],
  "children": [
    {
      "id": 12300,
      "label": "infantile convulsions and choreoathetosis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        4370,
        16273,
        16428,
        24281
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0008553",
          "MEDGEN:356123",
          "MESH:C535522",
          "NCIT:C126650",
          "OMIM:602066",
          "Orphanet:31709",
          "SCTID:715534008",
          "UMLS:C1865926"
        ],
        "synonyms": [
          "ICCA syndrome",
          "PKD/IC",
          "infantile convulsions and choreoathetosis",
          "paroxysmal kinesigenic dyskinesia and infantile convulsions",
          "ICCA",
          "Icca syndrome",
          "convulsions, familial infantile, with paroxysmal choreoathetosis",
          "convulsions, infantile, with paroxysmal choreoathetosis, familial",
          "infantile convulsions and paroxysmal choreoathetosis, familial",
          "paroxysmal kinesigenic dyskinesia with infantile convulsions"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A neurological condition characterized by the occurrence of seizures during the first year of life (Benign familial infantile epilepsy) and choreoathetotic dyskinetic attacks during childhood or adolescence."
      },
      "child_count": 0,
      "reference_id": "MONDO:0011178"
    },
    {
      "id": 16423,
      "label": "benign non-familial infantile seizures",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16428
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020071",
          "Orphanet:166295"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 2,
      "reference_id": "MONDO:0015637"
    },
    {
      "id": 16426,
      "label": "benign infantile seizures associated with mild gastroenteritis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16428
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020074",
          "MEDGEN:1647397",
          "Orphanet:166305",
          "SCTID:765756007",
          "UMLS:C4707564",
          "icd11.foundation:839512399"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Benign infantile seizures associated with mild gastroenteritis is a rare infantile epilepsy syndrome characterized by benign afebrile seizures in previously healthy infants and children (age range 1 month to 6 years) with mild acute gastroenteritis without any central nervous system infection, severe dehydration, or electrolyte imbalances. In most cases the seizures are tonic-clonic with focal origin on EEG, occur between day 1 and 6 following onset of acute gastroenteritis, cease within 24 hours and do not persist after the illness."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015640"
    },
    {
      "id": 16427,
      "label": "benign infantile focal epilepsy with midline spikes and wave during sleep",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        16428
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020075",
          "MEDGEN:1663004",
          "Orphanet:166308",
          "UMLS:C4749346"
        ],
        "synonyms": [
          "BIMSE",
          "benign infantile focal epilepsy with midline spikes and waves during sleep"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Benign infantile focal epilepsy with midline spikes and waves during sleep is a rare infantile epilepsy syndrome characterized by age of onset between 4 and 30 months, partial sporadic seizures presenting with motion arrest, staring, cyanosis and, less common, automatisms and lateralizing signs, and characteristic interictal sleep EEG changes consisting of a spike followed by a bell-shaped slow wave in the midline region."
      },
      "child_count": 0,
      "reference_id": "MONDO:0015641"
    },
    {
      "id": 17892,
      "label": "benign familial infantile epilepsy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        16428,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060169",
          "GARD:0000857",
          "ICD9:V17.2",
          "MEDGEN:1806836",
          "OMIMPS:601764",
          "Orphanet:306",
          "SCTID:230410004",
          "UMLS:C5575231",
          "icd11.foundation:1944845279"
        ],
        "synonyms": [
          "BFIE",
          "BFIS",
          "benign familial infantile convulsions",
          "benign familial infantile seizures",
          "seizures, benign familial infantile"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A genetic epileptic syndrome characterized by the occurrence of afebrile repeated seizures in healthy infants, between the third and eighth month of life."
      },
      "child_count": 10,
      "reference_id": "MONDO:0017615"
    }
  ],
  "roots": [
    {
      "id": 19724,
      "label": "infantile epilepsy syndrome"
    }
  ]
}