{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2019/G71.2",
    "parent": [
        "http://id.who.int/icd/release/10/2019/G71"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2019/en#/G71.2",
    "code": "G71.2",
    "title": {
        "@language": "en",
        "@value": "Congenital myopathies"
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Congenital muscular dystrophy: NOS"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Congenital muscular dystrophy: with specific morphological abnormalities of the muscle fibre"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Disease: central core"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Disease: minicore"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Disease: multicore"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Fibre-type disproportion"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Myopathy: myotubular (centronuclear)"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Myopathy: nemaline"
            }
        }
    ],
    "classKind": "category"
}