{
  "id": 11828,
  "label": "X-linked myopathy with excessive autophagy",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0010684",
  "properties": {
    "xrefs": [
      "DOID:0050760",
      "GARD:0003892",
      "MEDGEN:374264",
      "MESH:C536522",
      "NANDO:1200223",
      "NORD:1866",
      "OMIM:310440",
      "Orphanet:25980",
      "SCTID:719815005",
      "UMLS:C1839615"
    ],
    "synonyms": [
      "XMEA",
      "myopathy, X-linked, with excessive autophagy, X-linked recessive",
      "vacuolar myopathy",
      "MEAX",
      "myopathy, X-linked, with excessive autophagy"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "X-linked myopathy with excessive autophagy is a childhood-onset X-linked myopathy characterized by slow progression of muscle weakness and unique histopathological findings."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 16732,
      "label": "progressive muscular dystrophy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19744
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020360",
          "MEDGEN:1633060",
          "Orphanet:206644",
          "UMLS:C4551827"
        ],
        "synonyms": [
          "progressive muscular dystrophy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 13,
      "reference_id": "MONDO:0016106"
    },
    {
      "id": 16735,
      "label": "hereditary inclusion-body myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7023,
        24618
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020364",
          "MEDGEN:1843174",
          "Orphanet:206662",
          "UMLS:C5680794"
        ],
        "synonyms": [
          "inclusion myopathy",
          "cytoplasmic body myopathy"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          }
        ]
      },
      "child_count": 16,
      "reference_id": "MONDO:0016112"
    }
  ],
  "children": [
    {
      "id": 13343,
      "label": "myopathy, autophagic vacuolar, infantile-onset",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        11828
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0024858",
          "MEDGEN:419364",
          "OMIM:609500",
          "UMLS:C2931230"
        ],
        "synonyms": [
          "myopathy, autophagic vacuolar, infantile-onset"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 0,
      "reference_id": "MONDO:0012286"
    }
  ],
  "roots": [
    {
      "id": 16732,
      "label": "progressive muscular dystrophy"
    },
    {
      "id": 16735,
      "label": "hereditary inclusion-body myopathy"
    }
  ]
}