{
  "id": 22682,
  "label": "muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0033556",
  "properties": {
    "xrefs": [
      "DOID:0112376",
      "GARD:0025809",
      "MEDGEN:1755743",
      "OMIM:618992",
      "UMLS:C5436552"
    ],
    "synonyms": [
      "MDDGB15",
      "MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 15",
      "muscular dystrophy, congenital, DPM3-related"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2757,
      "label": "muscular dystrophy-dystroglycanopathy, type B",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18393
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0112375",
          "GARD:0012589",
          "OMIMPS:613155"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 8,
      "reference_id": "MONDO:0000172"
    },
    {
      "id": 14087,
      "label": "DPM3-congenital disorder of glycosylation",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7156,
        17978,
        18393
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0012395",
          "MEDGEN:414534",
          "MESH:C567857",
          "OMIM:612937",
          "Orphanet:263494",
          "SCTID:725044000",
          "UMLS:C2752007"
        ],
        "synonyms": [
          "CDG syndrome type Io",
          "CDG-Io",
          "CDG1O",
          "DPM3-CDG",
          "DPM3-congenital disorder of glycosylation",
          "carbohydrate deficient glycoprotein syndrome type Io",
          "congenital disorder of glycosylation type 1o",
          "congenital disorder of glycosylation type Io",
          "muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15",
          "CDG Io",
          "CDGIo",
          "Cdg1(Dpm3)",
          "DG1O",
          "DPM3-CDG (CDG-Io)",
          "congenital disorder of glycosylation, type Io"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "DPM3-CDG is an extremely rare form of CDG syndrome characterized clinically in the single reported case by muscle weakness, waddling gait and dilated cardiomyopathy."
      },
      "child_count": 3,
      "reference_id": "MONDO:0013049"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2757,
      "label": "muscular dystrophy-dystroglycanopathy, type B"
    },
    {
      "id": 14087,
      "label": "DPM3-congenital disorder of glycosylation"
    }
  ]
}