{
  "id": 10892,
  "label": "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4",
  "model": {
    "label": "Mondo Disease Ontology (MONDO)",
    "source": 0
  },
  "type_id": 0,
  "reference_id": "MONDO:0009678",
  "properties": {
    "xrefs": [
      "DOID:0050559",
      "GARD:0006475",
      "MEDGEN:140820",
      "NANDO:1200494",
      "NANDO:2200860",
      "NCIT:C126741",
      "NORD:1169",
      "OMIM:253800",
      "Orphanet:272",
      "SCTID:111502003",
      "UMLS:C0410174"
    ],
    "synonyms": [
      "FCMD",
      "Fukuyama Type Congenital Muscular Dystrophy",
      "Fukuyama congenital muscular dystrophy",
      "MDDGA4",
      "Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related",
      "muscle-eye-brain-FKTN related",
      "muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4",
      "muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4",
      "congenital muscular dystrophy, Fukuyama type"
    ],
    "categories": [
      {
        "ref": "MONDO:0002081",
        "name": "musculoskeletal system disorder"
      },
      {
        "ref": "MONDO:0005071",
        "name": "nervous system disorder"
      }
    ],
    "definition": "Fukuyama type muscular dystrophy (FCMD) is a congenital progressive muscular dystrophy characterized by brain malformation (cobblestone lissencephaly), dystrophic changes in skeletal muscle, severe intellectual deficit, epilepsy and motor impairment."
  },
  "isLeaf": true,
  "isRoot": false,
  "child_count": 0,
  "parents": [
    {
      "id": 2756,
      "label": "muscular dystrophy-dystroglycanopathy, type A",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        18393
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "DOID:0050560",
          "GARD:0002599",
          "MEDGEN:75553",
          "MESH:D058494",
          "NCIT:C99109",
          "OMIMPS:236670",
          "Orphanet:899",
          "SCTID:111504002",
          "UMLS:C0265221"
        ],
        "synonyms": [
          "WWS",
          "Walker-Warburg muscular dystrophy",
          "Walker-Warburg syndrome",
          "hard syndrome",
          "hydrocephalus-agyria-retinal dysplasia syndrome",
          "Chemke syndrome",
          "Pagon syndrome",
          "Warburg syndrome",
          "cerebroocular dysgenesis",
          "cerebroocular dysplasia muscular dystrophy syndrome",
          "hard +/- E syndrome",
          "hydrocephalus, agyria and retinal dysplasia"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ]
      },
      "child_count": 14,
      "reference_id": "MONDO:0000171"
    },
    {
      "id": 18861,
      "label": "muscle-eye-brain disease",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        19667
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0000156",
          "ICD9:742.4",
          "MEDGEN:105341",
          "Orphanet:588",
          "SCTID:277950001",
          "UMLS:C0457133"
        ],
        "synonyms": [
          "MEB syndrome",
          "Santavuori congenital muscular dystrophy",
          "muscle-eye-brain syndrome",
          "muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3",
          "MEB",
          "muscle eye brain disease"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "A rare, congenital muscular dystrophy due to dystroglycanopathy characterized by early onset muscular dystrophy, severe muscular hypotonia, severe mental retardation and typical brain and eye malformations, including pachygyria, polymicrogyria, agyria, brainstem and cerebellar structural anomalies, severe myopia, glaucoma, optic nerve and retinal hypoplasia. Patients may present with seizures, macrocephaly or microcephaly, microphthalmia, and congenital contractures. Depending on the severity, limited motor function is acquired. Less severe cases have been reported."
      },
      "child_count": 9,
      "reference_id": "MONDO:0018939"
    },
    {
      "id": 24463,
      "label": "myopathy caused by variation in FKTN",
      "isLeaf": false,
      "isRoot": false,
      "parents": [
        7023,
        16755,
        24618
      ],
      "type_id": 0,
      "properties": {
        "xrefs": [
          "GARD:0026340"
        ],
        "synonyms": [
          "FKTN myopathy",
          "FKTN-related myopathy",
          "myopathy caused by mutation in FKTN"
        ],
        "categories": [
          {
            "ref": "MONDO:0002081",
            "name": "musculoskeletal system disorder"
          },
          {
            "ref": "MONDO:0005071",
            "name": "nervous system disorder"
          }
        ],
        "definition": "Any myopathy in which the cause of the disease is a variation in the FKTN gene."
      },
      "child_count": 9,
      "reference_id": "MONDO:0700067"
    }
  ],
  "children": [],
  "roots": [
    {
      "id": 2756,
      "label": "muscular dystrophy-dystroglycanopathy, type A"
    },
    {
      "id": 18861,
      "label": "muscle-eye-brain disease"
    },
    {
      "id": 24463,
      "label": "myopathy caused by variation in FKTN"
    }
  ]
}