{
  "id": 24240,
  "label": "mirror movements 1 and/or agenesis of the corpus callosum",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0100515",
  "properties": {
    "xrefs": [
      "GARD:0026260"
    ],
    "categories": [
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "A familial congenital mirror movement disorder where individuals with heterozygous variants in DCC have congenital mirror movements and/or agenesis of the corpus callosum (not with or without- some individuals do not demonstrate mirror movements and only have corpus callosum defects, even within the same family)."
  },
  "isLeaf": false,
  "isRoot": false,
  "child_count": 1,
  "parents": [
    {
      "id": 17053,
      "label": "familial congenital mirror movements",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        4427,
        7073,
        24270
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0111153",
          "GARD:0012551",
          "MEDGEN:473166",
          "OMIMPS:157600",
          "Orphanet:238722",
          "SCTID:229247004",
          "UMLS:C0454455",
          "icd11.foundation:1966778637"
        ],
        "synonyms": [
          "familial congenital controlateral synkinesia",
          "familial congenital mirror movements",
          "hereditary congenital controlateral synkinesia",
          "hereditary congenital mirror movements",
          "isolated congenital controlateral synkinesia",
          "isolated congenital mirror movements",
          "CMM",
          "bimanual synkinesis",
          "congenital mirror movement disorder",
          "congenital mirror movements"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Congenital mirror movement disorder is a condition in which intentional movements of one side of the body are mirrored by involuntary movements of the other side. For example, when an affected individual makes a fist with the right hand, the left hand makes a similar movement. The mirror movements in this disorder primarily involve the upper limbs, especially the hands and fingers. This pattern of movements is present from infancy or early childhood and usually persists throughout life, without other associated signs and symptoms. Intelligence and lifespan are not affected."
      },
      "child_count": 12,
      "reference_id": "MONDO:0016558"
    }
  ],
  "children": [
    {
      "id": 9328,
      "label": "mirror movements 1",
      "isLeaf": true,
      "isRoot": false,
      "parents": [
        24240
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0070636",
          "GARD:0015086",
          "MEDGEN:320461",
          "OMIM:157600",
          "UMLS:C1834870"
        ],
        "synonyms": [
          "DCC familial congenital mirror movements",
          "familial congenital mirror movements caused by mutation in DCC",
          "mirror movements 1",
          "mirror movements type 1",
          "MRMV1",
          "bimanual synergia",
          "mirror movements 1 and/Or agenesis of the corpus callosum",
          "mirror movements, congenital"
        ],
        "categories": [
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene."
      },
      "child_count": 0,
      "reference_id": "MONDO:0008002"
    }
  ],
  "roots": [
    {
      "id": 17053,
      "label": "familial congenital mirror movements"
    }
  ]
}