{
  "id": 9431,
  "label": "Feingold syndrome type 1",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0008115",
  "properties": {
    "xrefs": [
      "GARD:0017624",
      "ICD9:759.89",
      "MEDGEN:1637716",
      "OMIM:164280",
      "Orphanet:391641",
      "SCTID:702431004",
      "UMLS:C4551774"
    ],
    "synonyms": [
      "Brunner-Winter syndrome type 1",
      "FGLDS1",
      "FS1",
      "Feingold syndrome caused by mutation in MYCN",
      "Feingold syndrome type 1",
      "MMT type 1",
      "MODED syndrome type 1",
      "MYCN Feingold syndrome",
      "ODED syndrome type 1",
      "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1",
      "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1",
      "microcephaly-digital anomalies-normal intelligence syndrome type 1",
      "microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1",
      "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1",
      "oculo-digito-esophageal-duodenal syndrome type 1",
      "Feingold syndrome",
      "Feingold syndrome 1",
      "Mmt syndrome",
      "Oded syndrome",
      "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
      "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum",
      "microcephaly and digital abnormalities with normal intelligence",
      "microcephaly, intellectual disability, and tracheoesophageal fistula syndrome",
      "microcephaly, mental retardation, and tracheoesophageal fistula syndrome",
      "microcephaly-oculo-digito-esophageal-duodenal syndrome",
      "oculodigitoesophagoduodenal syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      }
    ],
    "definition": "Feingold syndrome type 1 (FS1) is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16150,
      "label": "Feingold syndrome",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        4370
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0060464",
          "GARD:0008407",
          "MEDGEN:163209",
          "NCIT:C74987",
          "OMIMPS:164280",
          "Orphanet:1305",
          "UMLS:C0796068"
        ],
        "synonyms": [
          "Brunner-Winter syndrome",
          "FGLDS",
          "FS",
          "MMT",
          "MODED syndrome",
          "ODED syndrome",
          "digital anomalies with short palpebral fissures and atresia of esophagus or duodenum",
          "digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum",
          "microcephaly-digital anomalies-normal intelligence syndrome",
          "microcephaly-intellectual disability-tracheoesophageal fistula syndrome",
          "microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome",
          "oculo-digito-esophageal-duodenal syndrome",
          "digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "Feingold syndrome (FS), also known as oculo-digito-esophageal-duodenal (ODED) syndrome, is a rare inherited malformation syndrome characterized by microcephaly, short stature and numerous digital anomalies and is comprised of two subtypes: FS type 1 (FS1) and FS type 2 (FS2). FS1 is by far the most common form while FS2 has only been reported in 3 patients and has the same clinical characteristics as FS1, apart from the absence of gastrointestinal atresia and short palpebral fissures."
      },
      "child_count": 4,
      "reference_id": "MONDO:0015267"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16150,
      "label": "Feingold syndrome"
    }
  ]
}