{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2016/G60.0",
    "parent": [
        "http://id.who.int/icd/release/10/2016/G60"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2016/en#/G60.0",
    "code": "G60.0",
    "title": {
        "@language": "en",
        "@value": "Hereditary motor and sensory neuropathy"
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Disease: Charcot-Marie-Tooth"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Disease: D\u00e9jerine-Sottas"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Hereditary motor and sensory neuropathy, types I-IV"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Hypertrophic neuropathy of infancy"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Peroneal muscular atrophy (axonal type)(hypertrophic type)"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Roussy-L\u00e9vy syndrome"
            }
        }
    ],
    "classKind": "category"
}