{
  "id": 25901,
  "label": "dysraphic spinal cord lipoma",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0958260",
  "properties": {
    "xrefs": [
      "GARD:0026990",
      "MEDGEN:1853158",
      "Orphanet:645273",
      "UMLS:C5816731"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0003900",
        "name": "connective tissue disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A rare group of spinal cord lipoma characterized by the presence of extramedullary lipomatous mass located at any point along the spinal cord with or without a dural defect."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 4,
  "parents": [
    {
      "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": 3974,
      "label": "spinal cord lipoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5711,
        20625
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13743",
          "GARD:0023013",
          "ICD9:214.8",
          "MEDGEN:91131",
          "NANDO:2200815",
          "NCIT:C4619",
          "Orphanet:645276",
          "SCTID:189017000",
          "UMLS:C0347446"
        ],
        "synonyms": [
          "lipoma of spinal cord",
          "spinal cord lipoma"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A benign adipose tissue neoplasm of the spinal cord. It is usually associated with dysraphism in which the intraspinal component communicates with a subcutaneous lipoma through a defect in the posterior elements of the spine. Non-dysraphic intramedullary spinal cord lipomas are very rare."
      },
      "child_count": 4,
      "reference_id": "MONDO:0001790"
    }
  ],
  "children": [
    {
      "id": 25943,
      "label": "isolated transitional filum lipoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027020",
          "MEDGEN:1853141",
          "Orphanet:645322",
          "UMLS:C5816722"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare dysraphic abnormality characterized by the infiltration of fatty tissue localized in the filum terminale, with abnormal conus shape. The spinal cord is typically attenuated and the limit between its end and the fatty filum is hard to distinguish. There are no additional spinal cord malformation, but it can be associated with vertebral abnormalities, anorectal malformation or other syndromic condition. It is named transitional for its intermediate image between an isolated filum lipoma and a terminal conus region lipoma."
      },
      "child_count": 0,
      "reference_id": "MONDO:0958346"
    },
    {
      "id": 25944,
      "label": "isolated filum lipoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027021",
          "MEDGEN:1853135",
          "Orphanet:645325",
          "UMLS:C5816720"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare dysraphic abnormality characterized by the infiltration of fatty tissue localized in the filum terminale, thickens and loses its flexibility, with normal conus shape, regardless of conus level. There is no other spinal cord malformation associated, but it can be associated with extraspinal malformation (ex: anorectal malformation) or syndromic situation."
      },
      "child_count": 0,
      "reference_id": "MONDO:0958347"
    },
    {
      "id": 25946,
      "label": "dorsal spinal cord lipoma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        25901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027023",
          "MEDGEN:741207",
          "Orphanet:645362",
          "UMLS:C1827419"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare lipomatous, dysraphic malformation characterized by attachment to the dorsal surface of the spinal cord but not extending to the conus. It can be associated with others features such as a stalk and vertebral bone abnormalities."
      },
      "child_count": 0,
      "reference_id": "MONDO:0958349"
    },
    {
      "id": 25947,
      "label": "conus spinal cord lipoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        25901
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0027024",
          "MEDGEN:1853144",
          "Orphanet:645367",
          "UMLS:C5816712"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare lipomatous, dysraphic malformation characterized by lipoma located wholly or partially at the conus."
      },
      "child_count": 2,
      "reference_id": "MONDO:0958350"
    }
  ],
  "roots": [
    {
      "id": 3158,
      "label": "spina bifida occulta"
    },
    {
      "id": 3974,
      "label": "spinal cord lipoma"
    }
  ]
}