{
  "id": 9415,
  "label": "linear nevus sebaceous syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008097",
  "properties": {
    "xrefs": [
      "DOID:0111530",
      "GARD:0010291",
      "MEDGEN:1646345",
      "NCIT:C4678",
      "NORD:1692",
      "OMIM:163200",
      "Orphanet:2612",
      "UMLS:C4552097"
    ],
    "synonyms": [
      "Nevus Sebaceus Syndrome",
      "Nevus sebaceous of Jadassohn",
      "Nevus sebaceus of Jadassohn",
      "Nevus sebaceus syndrome",
      "Schimmelpenning syndrome",
      "Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic",
      "Solomon syndrome",
      "linear sebaceous Nevus",
      "organoid Nevus",
      "organoid nevus syndrome",
      "Epidermal Nevus syndrome, formerly",
      "JNP",
      "Jadassohn Nevus phakomatosis",
      "Jadassohn nevus phakomatosis",
      "SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome",
      "SFM",
      "SFM syndrome",
      "Schimmelpenning Feuerstein Mims syndrome",
      "Sfm syndrome",
      "epidermal nevus syndrome",
      "linear sebaceous Nevus syndrome",
      "organoid Nevus phakomatosis",
      "organoid nevus phakomatosis",
      "sebaceous Nevus syndrome, linear",
      "sebaceous nevus syndrome linear"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002051",
        "name": "integumentary system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Linear nevus sebaceous syndrome (LNSS) is characterized by the association of a large sebaceous nevus, usually appearing on the face or on the scalp, with a broad spectrum of abnormalities that may affect every organ system, including the central nervous system (brain neoplasms, hemimegalencephaly and lateral ventricle enlargement)."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 7993,
      "label": "hamartoma",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6798
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:3462",
          "EFO:1000634",
          "HP:0010566",
          "ICD9:759.6",
          "MEDGEN:6713",
          "MESH:D006222",
          "NCIT:C3075",
          "SCTID:400006008",
          "UMLS:C0018552"
        ],
        "synonyms": [
          "hamartoma",
          "hamartoma (disease)"
        ],
        "definition": "A benign and excessive tumor-like growth of mature cells and normal tissues which grow in a disorganized pattern."
      },
      "child_count": 13,
      "reference_id": "MONDO:0006499"
    },
    {
      "id": 19507,
      "label": "developmental defect during embryogenesis",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        20383
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "ICD9:759.7",
          "MEDGEN:1825997",
          "NCIT:C99267",
          "Orphanet:93890",
          "SCTID:400038003",
          "UMLS:C5680284"
        ],
        "synonyms": [
          "congenital malformation syndrome",
          "developmental defect during embryogenesis",
          "disorder of embryonic morphogenesis",
          "embryonic morphogenesis disease",
          "malformation syndrome",
          "rare developmental defect during embryogenesis"
        ],
        "definition": "A disease that has its basis in the disruption of embryonic morphogenesis."
      },
      "child_count": 52,
      "reference_id": "MONDO:0019755"
    },
    {
      "id": 19759,
      "label": "palpebral nevus",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6801,
        19758
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:65985",
          "NCIT:C3880",
          "Orphanet:98588",
          "SCTID:231827008",
          "UMLS:C0239460"
        ],
        "synonyms": [
          "eyelid nevus",
          "melanocytic nevus of skin of eyelid",
          "nevus of eyelid",
          "nevus of the eyelid",
          "skin of eyelid melanocytic nevus"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A melanocytic nevus that involves the skin of eyelid."
      },
      "child_count": 2,
      "reference_id": "MONDO:0020179"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714,
        6820
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MESH:D012873",
          "SCTID:239001006"
        ],
        "synonyms": [
          "disease, genetic skin",
          "diseases, genetic skin",
          "genetic skin disease",
          "genetic skin diseases",
          "genodermatosis",
          "skin disease, genetic"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          }
        ],
        "definition": "An instance of skin disease that is caused by a modification of the individual's genome."
      },
      "child_count": 228,
      "reference_id": "MONDO:0100118"
    },
    {
      "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": 7993,
      "label": "hamartoma"
    },
    {
      "id": 19507,
      "label": "developmental defect during embryogenesis"
    },
    {
      "id": 19759,
      "label": "palpebral nevus"
    },
    {
      "id": 23867,
      "label": "hereditary skin disorder"
    },
    {
      "id": 24270,
      "label": "hereditary neurological disease"
    }
  ]
}