{
  "id": 12136,
  "label": "Matthew-Wood syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011010",
  "properties": {
    "xrefs": [
      "DOID:0050819",
      "DOID:0111807",
      "GARD:0000713",
      "MEDGEN:318679",
      "MESH:C537768",
      "OMIM:601186",
      "Orphanet:2470",
      "SCTID:722458000",
      "UMLS:C1832661"
    ],
    "synonyms": [
      "MCOPS9",
      "Matthew-Wood syndrome",
      "anophthalmia-pulmonary hypoplasia syndrome",
      "microphthalmia syndromic type 9",
      "microphthalmia, syndromic type 9",
      "syndromic microphthalmia type 9",
      "Matthew Wood syndrome",
      "anophthalmia, clinical, with mild Facial Dysmorphism and variable malformations of the lung, heart, and diaphragm",
      "anophthalmia/microphthalmia and pulmonary hypoplasia",
      "clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations",
      "microphthalmia syndromic 9",
      "microphthalmia, isolated, with coloboma 8",
      "microphthalmia, syndromic 9",
      "pulmonary Hypoplasia-diaphragmatic hernia-anophthalmia-Cardiac defect",
      "pulmonary agenesis microphthalmi and diaphragmatic defect",
      "pulmonary agenesis, microphthalmia, and diaphragmatic defect",
      "spear syndrome"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0005087",
        "name": "respiratory system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "Matthew-Wood syndrome is a rare clinical entity including as main characteristics anophthalmia or severe microphthalmia, and pulmonary hypoplasia or aplasia."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18951
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019833",
          "MEDGEN:1842829",
          "Orphanet:102285",
          "UMLS:C5680373"
        ],
        "synonyms": [
          "MCA without intellectual disability",
          "multiple congenital anomalies without intellectual disability with or without dysmorphism"
        ]
      },
      "child_count": 168,
      "reference_id": "MONDO:0015161"
    },
    {
      "id": 16618,
      "label": "thoracic malformation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19706
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:1842414",
          "NANDO:2201008",
          "Orphanet:182108",
          "UMLS:C5680597"
        ],
        "categories": [
          {
            "ref": "MONDO:0005087",
            "name": "respiratory system disorder"
          }
        ]
      },
      "child_count": 15,
      "reference_id": "MONDO:0015929"
    },
    {
      "id": 16704,
      "label": "syndromic microphthalmia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4370,
        5714,
        20367
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0080636",
          "GARD:0020342",
          "MEDGEN:1826052",
          "OMIMPS:309800",
          "Orphanet:202948",
          "UMLS:C5679782"
        ],
        "synonyms": [
          "microphthalmia, syndromic",
          "syndrome associated with microphthalmia",
          "syndromic microphthalmia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A microphthalmia that is part of a larger syndrome."
      },
      "child_count": 57,
      "reference_id": "MONDO:0016073"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16089,
      "label": "multiple congenital anomalies/dysmorphic syndrome without intellectual disability"
    },
    {
      "id": 16618,
      "label": "thoracic malformation"
    },
    {
      "id": 16704,
      "label": "syndromic microphthalmia"
    }
  ]
}