{
  "id": 18439,
  "label": "secondary neonatal autoimmune disease",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0018356",
  "properties": {
    "xrefs": [
      "GARD:0021643",
      "MEDGEN:1842254",
      "Orphanet:398091",
      "UMLS:C5680041"
    ],
    "synonyms": [
      "Transplacentally acquired neonatal autoimmune disease"
    ],
    "categories": [
      {
        "ref": "MONDO:0005046",
        "name": "immune system disorder"
      }
    ]
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 6,
  "parents": [
    {
      "id": 8586,
      "label": "autoimmune disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6778
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:417",
          "EFO:0005809",
          "ICD9:279.4",
          "ICD9:279.49",
          "ICD9:720",
          "MEDGEN:2135",
          "MESH:D001327",
          "NCIT:C2889",
          "OBI:1110054",
          "OMIM:109100",
          "SCTID:85828009",
          "UMLS:C0004364"
        ],
        "synonyms": [
          "autoimmune disease",
          "autoimmune disease or disorder",
          "autoimmune disorder",
          "disease, autoimmune",
          "autoimmune hypersensitivity disease",
          "hypersensitivity reaction type II disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A disorder resulting from loss of function or tissue destruction of an organ or multiple organs, arising from humoral or cellular immune responses of the individual to their own tissue constituents. It may be systemic (e.g., systemic lupus erythematosus), or organ specific, (e.g., thyroiditis)."
      },
      "child_count": 47,
      "reference_id": "MONDO:0007179"
    }
  ],
  "children": [
    {
      "id": 18421,
      "label": "transient neonatal myasthenia gravis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        10902,
        18439
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021625",
          "ICD10CM:P94.0",
          "MEDGEN:96918",
          "NCIT:C117308",
          "Orphanet:391504",
          "UMLS:C0495465",
          "icd11.foundation:2096990223"
        ],
        "synonyms": [
          "neonatal myasthenia gravis",
          "NMG",
          "transient neonatal acquired myasthenia",
          "transient neonatal autoimmune myasthenia gravis"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Transient neonatal myasthenia gravis (MG) is a rare form of MG occurring in neonates born to mothers who have the disorder or specific circulating autoantibodies."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018326"
    },
    {
      "id": 18440,
      "label": "neonatal antiphospholipid syndrome",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18439,
        20262
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021644",
          "MEDGEN:1664921",
          "Orphanet:398097",
          "UMLS:C4751518"
        ],
        "synonyms": [
          "neonatal Hughes syndrome",
          "neonatal antiphospholipid antibody syndrome"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018357"
    },
    {
      "id": 18441,
      "label": "neonatal autoimmune hemolytic anemia",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18439,
        19736
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021645",
          "MEDGEN:1662969",
          "Orphanet:398109",
          "UMLS:C4751517"
        ],
        "synonyms": [
          "neonatal AHA",
          "neonatal AIHA"
        ],
        "categories": [
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          },
          {
            "ref": "MONDO:0005570",
            "name": "hematologic disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018358"
    },
    {
      "id": 18442,
      "label": "neonatal dermatomyositis",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        3005,
        16899,
        18439
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021646",
          "MEDGEN:1649267",
          "Orphanet:398117",
          "UMLS:C4751516"
        ],
        "synonyms": [
          "neonatal DM"
        ],
        "categories": [
          {
            "ref": "MONDO:0002051",
            "name": "integumentary system disorder"
          },
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018359"
    },
    {
      "id": 18443,
      "label": "neonatal lupus erythematosus",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        9248,
        18439
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "EFO:0004537",
          "GARD:0021647",
          "MEDGEN:98372",
          "MESH:C536397",
          "NCIT:C99236",
          "NORD:1495",
          "Orphanet:398124",
          "SCTID:95609003",
          "UMLS:C0409979",
          "icd11.foundation:213855225"
        ],
        "synonyms": [
          "Neonatal Lupus",
          "congenital lupus",
          "congenital lupus erythematosus",
          "neonatal SLE",
          "neonatal lupus",
          "neonatal lupus syndrome",
          "neonatal systemic lupus erythematosus"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ],
        "definition": "A self-limited skin rash that appears in the neonatal period and usually resolves in four to six months after birth. It is caused by placental transfer of maternal autoantibodies, usually anti-Ro antibody. In a minority of cases, it is associated with congenital heart block, hepatitis, or thrombocytopenia. The mothers of the affected babies may be asymptomatic or suffer from systemic lupus erythematosus, Sjogren's syndrome, or rheumatoid arthritis."
      },
      "child_count": 0,
      "reference_id": "MONDO:0018360"
    },
    {
      "id": 18444,
      "label": "neonatal scleroderma",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        18439,
        19180
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0021648",
          "MEDGEN:1652107",
          "Orphanet:398127",
          "UMLS:C4509425"
        ],
        "categories": [
          {
            "ref": "MONDO:0003900",
            "name": "connective tissue disorder"
          },
          {
            "ref": "MONDO:0005046",
            "name": "immune system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0018361"
    }
  ],
  "roots": [
    {
      "id": 8586,
      "label": "autoimmune disease"
    }
  ]
}