{
  "id": 9741,
  "label": "spina bifida",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008449",
  "properties": {
    "xrefs": [
      "DOID:0080016",
      "EFO:0003105",
      "HP:0002414",
      "ICD10CM:Q05",
      "ICD10WHO:Q05",
      "ICD9:741",
      "MEDGEN:38283",
      "MESH:D016135",
      "NCIT:C101214",
      "SCTID:67531005",
      "UMLS:C0080178",
      "icd11.foundation:2036217905"
    ],
    "synonyms": [
      "rachischisis",
      "spina bifida",
      "spina bifida (disease)",
      "spinal meningocele",
      "spinal myelocele",
      "spinal myelomeningocele",
      "NTD",
      "neural tube defects, susceptibility to"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A congenital neural tube defect in which vertebrae are not fully formed. It results in the protrusion of the spinal cord through the opening of the vertebrae."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 2,
  "parents": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6799
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2490",
          "ICD9:742",
          "MEDGEN:105425",
          "NCIT:C97172",
          "UMLS:C0497552"
        ],
        "synonyms": [
          "congenital abnormality of the nervous system",
          "congenital nervous system disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "An abnormality of the nervous system that is present at birth or detected in the neonatal period."
      },
      "child_count": 217,
      "reference_id": "MONDO:0002320"
    },
    {
      "id": 4611,
      "label": "spinal cord disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4657
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:319",
          "EFO:0009488",
          "ICD9:336.8",
          "ICD9:336.9",
          "MEDGEN:11550",
          "MESH:D013118",
          "NCIT:C97110",
          "SCTID:48522003",
          "UMLS:C0037928"
        ],
        "synonyms": [
          "disease of spinal cord",
          "disease of the spinal cord",
          "disease or disorder of spinal cord",
          "disorder of spinal cord",
          "spinal cord disease",
          "spinal cord disease or disorder",
          "spinal cord disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A disease involving the spinal cord."
      },
      "child_count": 10,
      "reference_id": "MONDO:0002545"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29380
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD10CM:Q00-Q99",
          "MEDGEN:1843482",
          "UMLS:C0694457"
        ],
        "definition": "Any disease or disorder that disrupts the process development of an anatomical structure. Can be due to genetic or environmental causes. Typically happens during embryogenesis, but also includes post-embryonic development."
      },
      "child_count": 190,
      "reference_id": "MONDO:0021147"
    }
  ],
  "children": [
    {
      "id": 3158,
      "label": "spina bifida occulta",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9741
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080073",
          "HP:0003298",
          "ICD10CM:Q76.0",
          "ICD9:756.17",
          "MEDGEN:36380",
          "MESH:D016136",
          "NCIT:C101044",
          "Orphanet:645202",
          "SCTID:76916001",
          "UMLS:C0080174",
          "icd11.foundation:449489594"
        ],
        "synonyms": [
          "closed spinal dysraphism",
          "spina bifida occulta",
          "spina bifida occulta (disease)"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "The mildest form of spina bifida, characterized by any of several neural tube defects which may go undetected until an x-ray is performed. Treatment is symptomatic."
      },
      "child_count": 2,
      "reference_id": "MONDO:0000859"
    },
    {
      "id": 19188,
      "label": "isolated spina bifida",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        9741
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0007673",
          "MedDRA:10041524",
          "Orphanet:823"
        ],
        "synonyms": [
          "isolated spina bifida (disease)",
          "nonsyndromic spina bifida (disease)",
          "cleft spine",
          "open spine"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A spina bifida (disease) that is not part of a larger syndrome."
      },
      "child_count": 4,
      "reference_id": "MONDO:0019351"
    }
  ],
  "roots": [
    {
      "id": 4427,
      "label": "congenital nervous system disorder"
    },
    {
      "id": 4611,
      "label": "spinal cord disorder"
    },
    {
      "id": 20383,
      "label": "disorder of development or morphogenesis"
    }
  ]
}