{
  "id": 8859,
  "label": "basal laminar drusen",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0007472",
  "properties": {
    "xrefs": [
      "DOID:0060746",
      "GARD:0015060",
      "MEDGEN:152676",
      "MESH:C563034",
      "OMIM:126700",
      "UMLS:C0730295"
    ],
    "synonyms": [
      "basal laminar drusen",
      "drusen of Bruch membrane",
      "drusen, cuticular",
      "drusen, early adult-onset, grouped"
    ],
    "categories": [
      {
        "ref": "MONDO:0002022",
        "name": "disorder of orbital region"
      },
      {
        "ref": "MONDO:0004995",
        "name": "cardiovascular disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      },
      {
        "ref": "MONDO:0024458",
        "name": "disorder of visual system"
      }
    ],
    "definition": "A retinal drusen characterized by yellow-white deposits (drusen) that accumulate beneath the retinal pigment epithelium on Bruch membrane and that has material basis in mutations in the CFH gene on chromosome 1q31.3."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 3860,
      "label": "retinal dystrophies primarily involving Bruch's membrane",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4072,
        19000,
        23165
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:13227",
          "GARD:0022986",
          "ICD9:362.77",
          "MEDGEN:1720702",
          "UMLS:C0154866"
        ],
        "synonyms": [
          "Bruch's membrane inherited retinal dystrophy",
          "inherited retinal dystrophy of Bruch's membrane"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0004995",
            "name": "cardiovascular disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "A retinal dystrophy with etiology arising from Bruch's membrane, the site of drusen generation."
      },
      "child_count": 3,
      "reference_id": "MONDO:0001666"
    },
    {
      "id": 8378,
      "label": "retinal drusen",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4301
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:2569",
          "EFO:1001155",
          "ICD9:362.57",
          "MEDGEN:20549",
          "MESH:D015593",
          "MedDRA:10062776",
          "SCTID:247153005",
          "UMLS:C0035312"
        ],
        "categories": [
          {
            "ref": "MONDO:0002022",
            "name": "disorder of orbital region"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          },
          {
            "ref": "MONDO:0024458",
            "name": "disorder of visual system"
          }
        ],
        "definition": "Colloid or hyaline bodies lying beneath the retinal pigment epithelium. They may occur either secondary to changes in the choroid that affect the pigment epithelium or as an autosomal dominant disorder of the retinal pigment epithelium."
      },
      "child_count": 3,
      "reference_id": "MONDO:0006949"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 3860,
      "label": "retinal dystrophies primarily involving Bruch's membrane"
    },
    {
      "id": 8378,
      "label": "retinal drusen"
    }
  ]
}