{
  "id": 13277,
  "label": "foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0012216",
  "properties": {
    "xrefs": [
      "DOID:0070531",
      "GARD:0017632",
      "MEDGEN:814203",
      "MESH:C563774",
      "OMIM:609218",
      "Orphanet:397618",
      "UMLS:C3807873"
    ],
    "synonyms": [
      "FHONDA syndrome",
      "foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome",
      "foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis",
      "foveal hypoplasia type 2",
      "FVH2",
      "foveal hypoplasia 2",
      "foveal hypoplasia 2 with optic nerve decussation defects and anterior segment dysgenesis without albinism",
      "foveal hypoplasia 2 with or without optic nerve misrouting and/or anterior segment dysgenesis"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0002254",
        "name": "syndromic disease"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 4370,
      "label": "syndromic disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        29379
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:225",
          "MEDGEN:11688",
          "MESH:D013577",
          "NCIT:C28193",
          "OGMS:0000086",
          "UMLS:C0039082"
        ],
        "synonyms": [
          "cluster, symptom",
          "clusters, symptom",
          "symptom cluster",
          "symptom clusters",
          "syndrome",
          "syndrome associated with disease or disorder",
          "syndromes",
          "syndromic disease",
          "syndromic disease or disorder"
        ],
        "categories": [
          {
            "ref": "MONDO:0002254",
            "name": "syndromic disease"
          }
        ],
        "definition": "A group of signs, symptoms, and clinicopathological characteristics that may or may not have a genetic basis and collectively define an abnormal condition."
      },
      "child_count": 1182,
      "reference_id": "MONDO:0002254"
    },
    {
      "id": 19084,
      "label": "inborn disorder of amino acid transport",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        6510
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0018948",
          "ICD9:270.0",
          "MEDGEN:541381",
          "Orphanet:79166",
          "SCTID:16784003",
          "UMLS:C0268641",
          "icd11.foundation:1631611896"
        ],
        "synonyms": [
          "inborn disorder of amino acid absorption and transport",
          "disorder of amino acid absorption and transport"
        ]
      },
      "child_count": 19,
      "reference_id": "MONDO:0019216"
    },
    {
      "id": 19769,
      "label": "hereditary optic neuropathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7019
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0019540",
          "MedDRA:10061323",
          "Orphanet:98671",
          "icd11.foundation:2452831"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0020249"
    },
    {
      "id": 23292,
      "label": "foveal hypoplasia",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        5714
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "MEDGEN:393047",
          "OMIMPS:136520",
          "UMLS:C2673946"
        ],
        "synonyms": [
          "FVH"
        ],
        "definition": "Underdevelopment of the fovea centralis."
      },
      "child_count": 4,
      "reference_id": "MONDO:0044203"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 4370,
      "label": "syndromic disease"
    },
    {
      "id": 19084,
      "label": "inborn disorder of amino acid transport"
    },
    {
      "id": 19769,
      "label": "hereditary optic neuropathy"
    },
    {
      "id": 23292,
      "label": "foveal hypoplasia"
    }
  ]
}