{
  "id": 12472,
  "label": "myopathy, myofibrillar, 9, with early respiratory failure",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0011362",
  "properties": {
    "xrefs": [
      "DOID:0111188",
      "GARD:0012591",
      "MEDGEN:350930",
      "MESH:C564377",
      "MESH:C566343",
      "OMIM:603689",
      "OMIM:607569",
      "Orphanet:178464",
      "Orphanet:34521",
      "SCTID:702373006",
      "SCTID:733490006",
      "UMLS:C1863599"
    ],
    "synonyms": [
      "ADMERF",
      "Edstrom myopathy",
      "Edström myopathy",
      "HIBM-ERF",
      "HMERF",
      "HMERF-ERF",
      "distal myopathy with early respiratory muscle involvement",
      "hereditary inclusion body myopathy with early respiratory failure",
      "hereditary proximal myopathy with early respiratory failure",
      "myofibrillar myopathy with early respiratory failure",
      "myopathy, distal, with early respiratory failure, autosomal dominant",
      "myopathy, proximal, with early respiratory muscle involvement"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ]
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "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": 16734,
      "label": "autosomal dominant distal myopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        18871
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0020361",
          "MEDGEN:1826097",
          "Orphanet:206650",
          "UMLS:C5680803"
        ],
        "synonyms": [
          "distal myopathy, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of distal myopathy."
      },
      "child_count": 30,
      "reference_id": "MONDO:0016108"
    },
    {
      "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"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        2903,
        23917
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026247"
        ],
        "synonyms": [
          "TTN-related myopathy, autosomal dominant"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Autosomal dominant form of TTN-related myopathy."
      },
      "child_count": 8,
      "reference_id": "MONDO:0100494"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 16732,
      "label": "progressive muscular dystrophy"
    },
    {
      "id": 16734,
      "label": "autosomal dominant distal myopathy"
    },
    {
      "id": 16735,
      "label": "hereditary inclusion-body myopathy"
    },
    {
      "id": 24220,
      "label": "autosomal dominant titinopathy"
    }
  ]
}