{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2008/H35.5",
    "parent": [
        "http://id.who.int/icd/release/10/2008/H35"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2008/en#/H35.5",
    "code": "H35.5",
    "title": {
        "@language": "en",
        "@value": "Hereditary retinal dystrophy"
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Dystrophy: retinal (albipunctate)(pigmentary)(vitelliform)"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Dystrophy: tapetoretinal"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Dystrophy: vitreoretinal"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Retinitis pigmentosa"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Stargardt's disease"
            }
        }
    ],
    "classKind": "category"
}