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                "id": "MONDO:0008234",
                "name": "multiple endocrine adenomatosis type 2a"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine adenomatosis type II"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine adenomatosis, type II"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine neoplasia IIA"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine neoplasia type 2A"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine neoplasia type II"
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            {
                "id": "MONDO:0008234",
                "name": "multiple endocrine neoplasia, type II"
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            {
                "id": "MONDO:0008234",
                "name": "ptc syndrome"
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            {
                "id": "MONDO:0008234",
                "name": "men-2A syndrome"
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                "id": "MONDO:0008234",
                "name": "multiple endocrine neoplasia, type IIA"
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            {
                "id": "MONDO:0008234",
                "name": "pheochromocytoma and amyloid producing medullary thyroid carcinoma"
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            {
                "id": "MIM:171400",
                "name": "Multiple neoplasia 2A"
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                "id": "DOID:0050431",
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            {
                "id": "DOID:0050431",
                "name": "ARVC"
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            {
                "id": "DOID:0050431",
                "name": "ARVC cardiomyopathy"
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            {
                "id": "DOID:0050431",
                "name": "ARVD"
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            {
                "id": "DOID:0050431",
                "name": "arrhythmogenic right ventricular dysplasia"
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            {
                "id": "DOID:0050431",
                "name": "right ventricular ACM"
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                "id": "MONDO:0007152",
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                "id": "MONDO:0007152",
                "name": "ARVC1"
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            {
                "id": "MONDO:0007152",
                "name": "ARVD1"
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            {
                "id": "MONDO:0007152",
                "name": "TGFB3 arrhythmogenic right ventricular cardiomyopathy"
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            {
                "id": "MONDO:0007152",
                "name": "arrhythmogenic right ventricular cardiomyopathy 1"
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            {
                "id": "MONDO:0007152",
                "name": "arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3"
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            {
                "id": "MONDO:0007152",
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            {
                "id": "MONDO:0007152",
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            {
                "id": "MONDO:0007152",
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            {
                "id": "MONDO:0007152",
                "name": "arrhythmogenic right ventricular dysplasia, familial, 1"
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            {
                "id": "MIM:107970",
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                "id": "MONDO:0012082",
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            {
                "id": "MONDO:0012082",
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                "id": "MONDO:0012119",
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                "id": "MONDO:0012119",
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                "id": "MONDO:0012119",
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            {
                "id": "MONDO:0012119",
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                "id": "MONDO:0012377",
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                "id": "MONDO:0012377",
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                "id": "MONDO:0012377",
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            {
                "id": "MONDO:0012377",
                "name": "ASPERGER syndrome, susceptibility to, 4"
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                "id": "MONDO:0010808",
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                "id": "MONDO:0010808",
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                "id": "MONDO:0010808",
                "name": "Insomnia familial fatal"
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            {
                "id": "MONDO:0010808",
                "name": "familial fatal insomnia"
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            {
                "id": "MIM:600072",
                "name": "Fatal familial insomnia"
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                "id": "DOID:0050434",
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            {
                "id": "DOID:0050434",
                "name": "Andersen syndrome"
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                "id": "DOID:0050434",
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            {
                "id": "DOID:0050434",
                "name": "Long QT syndrome 7"
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            {
                "id": "DOID:0050434",
                "name": "Potassium-Sensitive Cardiodysrhythmic Type"
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            {
                "id": "MONDO:0008222",
                "name": "Andersen-Tawil syndrome"
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            {
                "id": "MONDO:0008222",
                "name": "ATS"
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            {
                "id": "MONDO:0008222",
                "name": "Andersen cardiodysrhythmic periodic paralysis"
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            {
                "id": "MONDO:0008222",
                "name": "Andersen syndrome"
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            {
                "id": "MONDO:0008222",
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                "id": "MONDO:0008222",
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            {
                "id": "MONDO:0008222",
                "name": "long QT syndrome 7"
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            {
                "id": "MONDO:0008222",
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            {
                "id": "MONDO:0008222",
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            {
                "id": "MIM:170390",
                "name": "Long QT syndrome 7"
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                "id": "DOID:0050436",
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                "id": "DOID:0050436",
                "name": "Mulibrey growth disorder"
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            {
                "id": "DOID:0050436",
                "name": "Muscle-Liver-Brain-Eye Nanism"
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                "id": "DOID:0050436",
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            {
                "id": "DOID:0050436",
                "name": "Perheentupa Syndrome"
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                "id": "MONDO:0009664",
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            {
                "id": "MONDO:0009664",
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            {
                "id": "MONDO:0009664",
                "name": "Perheentupa syndrome"
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                "id": "MONDO:0009664",
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            {
                "id": "MONDO:0009664",
                "name": "mulibrey nanism"
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            {
                "id": "MONDO:0009664",
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                "id": "MONDO:0009664",
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                "id": "MONDO:0009664",
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                "id": "MIM:253250",
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                "id": "DOID:0050437",
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                "id": "MONDO:0010281",
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            {
                "id": "MONDO:0010281",
                "name": "LAMP2 lysosomal glycogen storage disease"
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                "id": "MONDO:0010281",
                "name": "glycogen storage disease type IIb"
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                "id": "MONDO:0010281",
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            {
                "id": "MONDO:0010281",
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            {
                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0010281",
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                "id": "MONDO:0007635",
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                "id": "MONDO:0700087",
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                "id": "MIM:276900",
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                "id": "DOID:0050440",
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                "id": "MONDO:0007906",
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                "id": "MONDO:0007906",
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                "id": "MONDO:0007906",
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                "id": "MIM:151660",
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                "id": "DOID:0050441",
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                "id": "MIM:272200",
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                "id": "DOID:0050445",
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                "id": "DOID:0050445",
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                "id": "MONDO:0010619",
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            {
                "id": "MONDO:0010619",
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                "id": "MONDO:0010619",
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            {
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                "id": "MONDO:0010619",
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                "id": "MONDO:0010619",
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                "id": "MONDO:0010619",
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                "id": "MONDO:0010619",
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                "id": "MIM:307800",
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    {
        "record_id": "doid.0050448",
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                "id": "MONDO:0008086",
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                "id": "MONDO:0008086",
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                "id": "DOID:0050553",
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                "id": "MONDO:0054698",
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            {
                "id": "MONDO:0054698",
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                "id": "MIM:256040",
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                "id": "DOID:0050554",
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            {
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            {
                "id": "MONDO:0010524",
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            {
                "id": "MONDO:0010524",
                "name": "Pagon-Bird-Detter syndrome"
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            {
                "id": "MONDO:0010524",
                "name": "X-linked sideroblastic anaemia with spinocerebellar ataxia"
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            {
                "id": "MONDO:0010524",
                "name": "X-linked sideroblastic anemia with ataxia"
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            {
                "id": "MONDO:0010524",
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            {
                "id": "MONDO:0010524",
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            {
                "id": "MONDO:0010524",
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                "id": "MONDO:0010524",
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                "id": "MONDO:0010524",
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                "id": "MONDO:0010524",
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                "id": "MONDO:0010524",
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                "id": "MONDO:0010524",
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                "id": "MONDO:0007919",
                "name": "Milroy disease"
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                "id": "MONDO:0007919",
                "name": "Nonne-Milroy disease"
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            {
                "id": "MONDO:0007919",
                "name": "Nonne-Milroy lymphedema"
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            {
                "id": "MONDO:0007919",
                "name": "Nonne-Milroy syndrome"
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            {
                "id": "MONDO:0007919",
                "name": "Nonnes syndrome"
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            {
                "id": "MONDO:0007919",
                "name": "congenital hereditary lymphedema"
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            {
                "id": "MONDO:0007919",
                "name": "early onset lymphedema"
            },
            {
                "id": "MONDO:0007919",
                "name": "hereditary lymphedema 1"
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            {
                "id": "MONDO:0007919",
                "name": "hereditary lymphedema caused by mutation in FLT4"
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            {
                "id": "MONDO:0007919",
                "name": "hereditary lymphedema type I"
            },
            {
                "id": "MONDO:0007919",
                "name": "lymphedema, early-onset"
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            {
                "id": "MONDO:0007919",
                "name": "lymphedema, hereditary, 1A"
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            {
                "id": "MONDO:0007919",
                "name": "lymphedema, hereditary, type 1A"
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            {
                "id": "MONDO:0007919",
                "name": "primary congenital lymphedema"
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            {
                "id": "MIM:153100",
                "name": "Lymphatic malformation 1"
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                "id": "MONDO:0012071",
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                "id": "MONDO:0012071",
                "name": "AGPAT2 congenital generalised lipodystrophy (disease)"
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            {
                "id": "MONDO:0012071",
                "name": "AGPAT2 congenital generalized lipodystrophy (disease)"
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            {
                "id": "MONDO:0012071",
                "name": "BSCL1"
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            {
                "id": "MONDO:0012071",
                "name": "Berardinelli-Seip congenital lipodystrophy, type 1"
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            {
                "id": "MONDO:0012071",
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            {
                "id": "MONDO:0012071",
                "name": "congenital generalised lipodystrophy (disease) caused by mutation in AGPAT2"
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            {
                "id": "MONDO:0012071",
                "name": "congenital generalized lipodystrophy (disease) caused by mutation in AGPAT2"
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            {
                "id": "MONDO:0012071",
                "name": "congenital generalized lipodystrophy type 1"
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            {
                "id": "MONDO:0012071",
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            {
                "id": "MONDO:0012071",
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            {
                "id": "MONDO:0012071",
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                "id": "MIM:608594",
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                "id": "MONDO:0013189",
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            {
                "id": "MONDO:0013189",
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            {
                "id": "MIM:613229",
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            {
                "id": "MONDO:0013159",
                "name": "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1"
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                "id": "MIM:613155",
                "name": "Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B1"
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                "id": "MONDO:0009960",
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                "id": "MONDO:0009960",
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                "id": "MONDO:0009960",
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                "id": "MONDO:0009960",
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                "id": "MIM:266600",
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                "id": "MONDO:0007072",
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                "id": "DOID:0050633",
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                "id": "DOID:0050633",
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                "id": "MONDO:0021019",
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                "id": "MONDO:0021019",
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                "id": "MONDO:0021019",
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            {
                "id": "MONDO:0021019",
                "name": "XLOA"
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            {
                "id": "MONDO:0021019",
                "name": "ocular albinism type 1"
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                "id": "MONDO:0021019",
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                "id": "MONDO:0021019",
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                "id": "MONDO:0021019",
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            {
                "id": "MONDO:0021019",
                "name": "albinism, ocular, type I"
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            {
                "id": "MIM:300500",
                "name": "Albinism ocular 1"
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                "id": "DOID:0050634",
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                "id": "MONDO:0008757",
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                "id": "MONDO:0008757",
                "name": "AU"
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                "id": "MONDO:0008757",
                "name": "alopecia areata universalis"
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            {
                "id": "MIM:203655",
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                "id": "MONDO:0007087",
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                "id": "MONDO:0007087",
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                "id": "MONDO:0013900",
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                "id": "MONDO:0013900",
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                "id": "MONDO:0013900",
                "name": "alternating hemiplegia of childhood 2"
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                "id": "MONDO:0013900",
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                "id": "MONDO:0013900",
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                "id": "MONDO:0013900",
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                "id": "MIM:104290",
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                "id": "MIM:614820",
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                "id": "DOID:0050636",
                "name": "German type amyloidosis"
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                "id": "DOID:0050636",
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                "id": "DOID:0050636",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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            {
                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MONDO:0007099",
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                "id": "MIM:105200",
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                "id": "DOID:0050637",
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                "id": "DOID:0050638",
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                "id": "MONDO:0007157",
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            {
                "id": "DOID:0050647",
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                "id": "DOID:0050647",
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            {
                "id": "DOID:0050647",
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            {
                "id": "DOID:0050647",
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            {
                "id": "DOID:0050647",
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            {
                "id": "DOID:0050647",
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            {
                "id": "MONDO:0010533",
                "name": "Arts syndrome"
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                "id": "MONDO:0010533",
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                "id": "MONDO:0010533",
                "name": "Arts"
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            {
                "id": "MONDO:0010533",
                "name": "Arts syndrome"
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                "id": "MONDO:0010533",
                "name": "Arts syndrome, X-linked recessive"
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            {
                "id": "MONDO:0010533",
                "name": "MRXS18"
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                "id": "MONDO:0010533",
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                "id": "MONDO:0010533",
                "name": "lethal ataxia with deafness and optic atrophy"
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                "id": "MONDO:0010533",
                "name": "syndromic X-linked intellectual disability 18"
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                "id": "MONDO:0010533",
                "name": "syndromic X-linked intellectual disability Arts type"
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            {
                "id": "MONDO:0010533",
                "name": "X-linked fatal ataxia with deafness and loss of vision"
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                "id": "MONDO:0010533",
                "name": "lethal ataxia-deafness-optic atrophy"
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                "id": "MONDO:0010533",
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                "id": "MONDO:0010533",
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                "id": "MONDO:0007167",
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            {
                "id": "MONDO:0007167",
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                "id": "MONDO:0007167",
                "name": "spondylo-humero-femoral dysplasia"
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                "id": "MONDO:0007167",
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                "id": "MONDO:0007168",
                "name": "atelosteogenesis type III"
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                "id": "MONDO:0007168",
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                "id": "MONDO:0007168",
                "name": "atelosteogenesis type 3"
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            {
                "id": "MONDO:0007168",
                "name": "atelosteogenesis, type III"
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                "id": "MONDO:0009727",
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                "id": "MONDO:0009727",
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                "name": "AOII"
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                "id": "MONDO:0009727",
                "name": "atelosteogenesis type II"
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            {
                "id": "MONDO:0009727",
                "name": "neonatal osseous dysplasia type 1"
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                "id": "MONDO:0009727",
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                "id": "MONDO:0009727",
                "name": "atelosteogenesis, type II"
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                "id": "MIM:108720",
                "name": "Atelosteogenesis 1"
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                "id": "MIM:108721",
                "name": "Atelosteogenesis 3"
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            {
                "id": "MIM:256050",
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                "id": "MONDO:0008846",
                "name": "atransferrinemia"
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            {
                "id": "MONDO:0008846",
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            {
                "id": "MONDO:0008846",
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            {
                "id": "MONDO:0008846",
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            {
                "id": "MONDO:0008846",
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            {
                "id": "MIM:209300",
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            {
                "id": "MONDO:0012677",
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                "id": "MONDO:0012816",
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                "id": "MONDO:0012816",
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                "name": "familial atrial fibrillation caused by mutation in GJA5"
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                "id": "MONDO:0013545",
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                "id": "MIM:612240",
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                "id": "MONDO:0009437",
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                "id": "MIM:241850",
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                "id": "MONDO:0010305",
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                "id": "MONDO:0010305",
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                "id": "MONDO:0010305",
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                "id": "MONDO:0010305",
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                "id": "MONDO:0010305",
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                "id": "MONDO:0010305",
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                "name": "Ehlers-Danlos syndrome progeroid type"
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                "id": "MONDO:0014139",
                "name": "Ehlers-Danlos syndrome, spondylodysplastic type, 2"
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                "id": "MONDO:0014139",
                "name": "B3GALT6 Ehlers-Danlos syndrome progeroid type"
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                "id": "MONDO:0014139",
                "name": "B3GALT6-related spEDS"
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                "id": "MONDO:0014139",
                "name": "B3GALT6-related spondylodysplastic EDS"
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                "id": "MONDO:0014139",
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                "id": "MONDO:0014139",
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                "id": "MONDO:0014139",
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                "id": "MONDO:0014139",
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                "id": "MIM:615349",
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                "id": "MIM:612713",
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                "id": "DOID:0050811",
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                "id": "MIM:257920",
                "name": "3MC syndrome 1"
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                "id": "MONDO:0014124",
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                "id": "MONDO:0014124",
                "name": "Adams-Oliver syndrome 4"
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                "id": "MONDO:0014124",
                "name": "Adams-Oliver syndrome caused by mutation in EOGT"
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                "id": "MONDO:0014124",
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                "id": "MONDO:0014124",
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                "id": "MONDO:0014124",
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                "id": "MONDO:0014459",
                "name": "Adams-Oliver syndrome 5"
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                "id": "MONDO:0014459",
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            {
                "id": "MONDO:0014459",
                "name": "Adams-Oliver syndrome 5"
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                "id": "MONDO:0014459",
                "name": "Adams-Oliver syndrome caused by mutation in NOTCH1"
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            {
                "id": "MONDO:0014459",
                "name": "Adams-Oliver syndrome caused by mutation in Notch1"
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                "id": "MONDO:0014459",
                "name": "Adams-Oliver syndrome type 5"
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                "id": "MONDO:0024506",
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                "id": "MONDO:0024506",
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                "id": "MIM:614219",
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                "id": "MIM:615297",
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                "id": "MIM:616028",
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                "id": "MIM:100300",
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                "id": "MONDO:0009470",
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                "id": "MONDO:0009470",
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                "id": "MONDO:0009470",
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                "id": "MIM:243310",
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                "id": "MONDO:0007247",
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                "id": "MONDO:0007247",
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                "id": "MONDO:0009806",
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                "id": "MONDO:0009806",
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                "id": "MIM:278300",
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                "id": "MONDO:0010822",
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                "id": "MIM:600118",
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                "id": "MIM:601390",
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                "id": "MONDO:0011712",
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                "id": "MONDO:0010909",
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                "id": "MONDO:0010909",
                "name": "UVSS1"
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                "id": "MONDO:0010559",
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                "id": "MIM:303350",
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                "id": "DOID:0060248",
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                "id": "MONDO:0020602",
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                "id": "DOID:0060394",
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                "id": "MONDO:0012774",
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                "id": "MONDO:0012774",
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                "id": "MIM:613406",
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            },
            {
                "id": "MIM:616294",
                "name": "Cole-Carpenter syndrome 2"
            }
        ],
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    {
        "record_id": "doid.0060439",
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            {
                "id": "DOID:0060439",
                "name": "LPI"
            },
            {
                "id": "DOID:0060439",
                "name": "dibasic amino aciduria II"
            },
            {
                "id": "DOID:0060439",
                "name": "hyperdibasic aminoaciduria"
            },
            {
                "id": "MONDO:0009109",
                "name": "lysinuric protein intolerance"
            },
            {
                "id": "MONDO:0009109",
                "name": "LPI"
            },
            {
                "id": "MONDO:0009109",
                "name": "hyperdibasic aminoaciduria"
            },
            {
                "id": "MONDO:0009109",
                "name": "hyperdibasic aminoaciduria type 2"
            },
            {
                "id": "MONDO:0009109",
                "name": "lysinuric protein intolerance"
            },
            {
                "id": "MONDO:0009109",
                "name": "Dibasicamino aciduria II"
            },
            {
                "id": "MONDO:0009109",
                "name": "dibasic aminoaciduria 2"
            },
            {
                "id": "MIM:222700",
                "name": "Lysinuric protein intolerance"
            }
        ],
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        "record_type": "disease"
    },
    {
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        "disease_id": "DOID:0060444",
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            {
                "id": "DOID:0060444",
                "name": "CGD2"
            },
            {
                "id": "DOID:0060444",
                "name": "avellino corneal dystrophy"
            },
            {
                "id": "DOID:0060444",
                "name": "combined granular-lattice corneal dystrophy"
            },
            {
                "id": "DOID:0060444",
                "name": "corneal dystrophy, Avellino type"
            },
            {
                "id": "DOID:0060444",
                "name": "granular corneal dystrophy type 2"
            },
            {
                "id": "MONDO:0011855",
                "name": "granular corneal dystrophy type II"
            },
            {
                "id": "MONDO:0011855",
                "name": "Avellino corneal dystrophy"
            },
            {
                "id": "MONDO:0011855",
                "name": "CGD2"
            },
            {
                "id": "MONDO:0011855",
                "name": "GCD2"
            },
            {
                "id": "MONDO:0011855",
                "name": "GCDII"
            },
            {
                "id": "MONDO:0011855",
                "name": "avellino corneal dystrophy"
            },
            {
                "id": "MONDO:0011855",
                "name": "combined granular-lattice corneal dystrophy"
            },
            {
                "id": "MONDO:0011855",
                "name": "granular corneal dystrophy type 2"
            },
            {
                "id": "MONDO:0011855",
                "name": "granular-lattice corneal dystrophy"
            },
            {
                "id": "MONDO:0011855",
                "name": "ACD"
            },
            {
                "id": "MONDO:0011855",
                "name": "CDA"
            },
            {
                "id": "MONDO:0011855",
                "name": "combined granular-lattice corneal dystrophies"
            },
            {
                "id": "MONDO:0011855",
                "name": "corneal dystrophy Avellino type"
            },
            {
                "id": "MONDO:0011855",
                "name": "corneal dystrophy, AVELLINO type"
            },
            {
                "id": "MONDO:0011855",
                "name": "granular and lattice corneal dystrophies"
            },
            {
                "id": "MONDO:0011855",
                "name": "granular-lattice (Avellino) corneal dystrophy"
            },
            {
                "id": "MIM:607541",
                "name": "Corneal dystrophy, Avellino type"
            }
        ],
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        "record_type": "disease"
    },
    {
        "record_id": "doid.0060445",
        "disease_id": "DOID:0060445",
        "recommended_name": "congenital stromal corneal dystrophy",
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            {
                "id": "DOID:0060445",
                "name": "CSCD"
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            {
                "id": "DOID:0060445",
                "name": "congenital hereditary stromal dystrophy"
            },
            {
                "id": "MONDO:0012401",
                "name": "congenital stromal corneal dystrophy"
            },
            {
                "id": "MONDO:0012401",
                "name": "CSCD"
            },
            {
                "id": "MONDO:0012401",
                "name": "Witschel dystrophy"
            },
            {
                "id": "MONDO:0012401",
                "name": "congenital hereditary stromal dystrophy"
            },
            {
                "id": "MONDO:0012401",
                "name": "congenital stromal corneal dystrophy"
            },
            {
                "id": "MONDO:0012401",
                "name": "corneal dystrophy, congenital stromal"
            },
            {
                "id": "MIM:610048",
                "name": "Corneal dystrophy, congenital stromal"
            }
        ],
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        "record_type": "disease"
    },
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            {
                "id": "DOID:0060447",
                "name": "Cogan corneal dystrophy"
            },
            {
                "id": "DOID:0060447",
                "name": "EBMD"
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            {
                "id": "DOID:0060447",
                "name": "microcystic corneal dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "epithelial basement membrane dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "Cogan corneal dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "Cogan microcystic epithelial dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "EBMD"
            },
            {
                "id": "MONDO:0007375",
                "name": "Map-dot-fingerprint dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "anterior basement membrane dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "Map-dot-fingerprint dystrophy of cornea"
            },
            {
                "id": "MONDO:0007375",
                "name": "corneal dystrophy, epithelial basement MEMBRANE"
            },
            {
                "id": "MONDO:0007375",
                "name": "epithelial basement membrane corneal dystrophy"
            },
            {
                "id": "MONDO:0007375",
                "name": "microcystic dystrophy of the cornea"
            },
            {
                "id": "MIM:121820",
                "name": "Corneal dystrophy, epithelial basement membrane"
            }
        ],
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    {
        "record_id": "doid.0060448",
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        "recommended_name": "Fleck corneal dystrophy",
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            {
                "id": "DOID:0060448",
                "name": "FCD"
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            {
                "id": "DOID:0060448",
                "name": "Francois-Neetens speckled corneal dystrophy"
            },
            {
                "id": "MONDO:0007376",
                "name": "fleck corneal dystrophy"
            },
            {
                "id": "MONDO:0007376",
                "name": "FCD"
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            {
                "id": "MONDO:0007376",
                "name": "FranC'ois-Neetens speckled corneal dystrophy"
            },
            {
                "id": "MONDO:0007376",
                "name": "Franois-Neetens speckled corneal dystrophy"
            },
            {
                "id": "MONDO:0007376",
                "name": "corneal fleck dystrophy"
            },
            {
                "id": "MONDO:0007376",
                "name": "fleck corneal dystrophy"
            },
            {
                "id": "MIM:121850",
                "name": "Corneal dystrophy, fleck"
            }
        ],
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            {
                "id": "DOID:0060449",
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                "id": "DOID:0060449",
                "name": "corneal amyloidosis"
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                "id": "DOID:0060449",
                "name": "primary familial amyloidosis of the cornea"
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            {
                "id": "DOID:0060449",
                "name": "subepithelial amyloidosis of the cornea"
            },
            {
                "id": "MONDO:0008777",
                "name": "gelatinous drop-like corneal dystrophy"
            },
            {
                "id": "MONDO:0008777",
                "name": "GDCD"
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            {
                "id": "MONDO:0008777",
                "name": "corneal amyloidosis"
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            {
                "id": "MONDO:0008777",
                "name": "gelatinous drop-like corneal dystrophy"
            },
            {
                "id": "MONDO:0008777",
                "name": "primary familial amyloidosis of the cornea"
            },
            {
                "id": "MONDO:0008777",
                "name": "subepithelial amyloidosis of the cornea"
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            {
                "id": "MONDO:0008777",
                "name": "CDGDL"
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            {
                "id": "MONDO:0008777",
                "name": "GDLD"
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            {
                "id": "MONDO:0008777",
                "name": "amyloid corneal dystrophy, Japanese type"
            },
            {
                "id": "MONDO:0008777",
                "name": "amyloidosis corneal"
            },
            {
                "id": "MONDO:0008777",
                "name": "corneal dystrophy, gelatinous drop-like"
            },
            {
                "id": "MONDO:0008777",
                "name": "corneal dystrophy, lattice type 3"
            },
            {
                "id": "MONDO:0008777",
                "name": "lattice corneal dystrophy type 3"
            },
            {
                "id": "MIM:204870",
                "name": "Corneal dystrophy, gelatinous drop-like"
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        ],
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                "id": "DOID:0060450",
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                "id": "DOID:0060450",
                "name": "band-shaped and whorled microcystic"
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            {
                "id": "MONDO:0010425",
                "name": "Lisch epithelial corneal dystrophy"
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                "id": "MONDO:0010425",
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            {
                "id": "MONDO:0010425",
                "name": "Lisch epithelial corneal dystrophy"
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            {
                "id": "MONDO:0010425",
                "name": "band-shaped and whorled microcystic dystrophy of the corneal epithelium"
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            {
                "id": "MONDO:0010425",
                "name": "corneal dystrophy, Lisch epithelial, X-linked dominant"
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            {
                "id": "MONDO:0010425",
                "name": "corneal dystrophy, Lisch epithelial"
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            {
                "id": "MONDO:0010425",
                "name": "Lisch epithelial corneal dystrophy"
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                "id": "MONDO:0010425",
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            {
                "id": "MONDO:0010425",
                "name": "Lisch epithelial corneal dystrophy"
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                "id": "MONDO:0010425",
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            },
            {
                "id": "MONDO:0010425",
                "name": "corneal dystrophy, Lisch epithelial, X-linked dominant"
            },
            {
                "id": "MONDO:0010425",
                "name": "corneal dystrophy, Lisch epithelial"
            },
            {
                "id": "MIM:620763",
                "name": "Corneal dystrophy, Lisch epithelial"
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                "id": "DOID:0060451",
                "name": "MECD"
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            {
                "id": "DOID:0060451",
                "name": "Stocker-Holt dystrophy"
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            {
                "id": "DOID:0060451",
                "name": "juvenile hereditary epithelial dystrophy"
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            {
                "id": "MONDO:0020791",
                "name": "corneal dystrophy, Meesmann, 1"
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            {
                "id": "MONDO:0020791",
                "name": "MECD1"
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            {
                "id": "MIM:122100",
                "name": "Corneal dystrophy, Meesmann 1"
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                "id": "DOID:0060453",
                "name": "RBCD"
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                "id": "DOID:0060453",
                "name": "anterior limiting membrane dystrophy type I"
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            {
                "id": "DOID:0060453",
                "name": "corneal dystrophy of Bowman layer type I"
            },
            {
                "id": "DOID:0060453",
                "name": "geographic corneal dystrophy"
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            {
                "id": "DOID:0060453",
                "name": "granular corneal dystrophy type III"
            },
            {
                "id": "MONDO:0012043",
                "name": "Reis-Bucklers corneal dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "RBCD"
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            {
                "id": "MONDO:0012043",
                "name": "Reis-Bucklers corneal dystrophy"
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                "id": "MONDO:0012043",
                "name": "anterior limiting membrane dystrophy type 1"
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            {
                "id": "MONDO:0012043",
                "name": "anterior limiting membrane dystrophy type I"
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            {
                "id": "MONDO:0012043",
                "name": "atypical granular corneal dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "corneal dystrophy of Bowman layer type 1"
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            {
                "id": "MONDO:0012043",
                "name": "corneal dystrophy of Bowman layer type I"
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            {
                "id": "MONDO:0012043",
                "name": "geographic corneal dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "granular corneal dystrophy type 3"
            },
            {
                "id": "MONDO:0012043",
                "name": "granular corneal dystrophy type III"
            },
            {
                "id": "MONDO:0012043",
                "name": "superficial granular corneal dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "CDB1"
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            {
                "id": "MONDO:0012043",
                "name": "CDRB"
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            {
                "id": "MONDO:0012043",
                "name": "Reis Bucklers corneal dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "Reis Bucklers dystrophy"
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            {
                "id": "MONDO:0012043",
                "name": "corneal dystrophy Reis Bucklers type"
            },
            {
                "id": "MONDO:0012043",
                "name": "corneal dystrophy geographic"
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            {
                "id": "MONDO:0012043",
                "name": "corneal dystrophy, REIS-Bucklers type"
            },
            {
                "id": "MIM:608470",
                "name": "Corneal dystrophy, Reis-Bucklers type"
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        ],
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            {
                "id": "DOID:0060455",
                "name": "TBCD"
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            {
                "id": "DOID:0060455",
                "name": "Waardenburg-Jonker corneal dystrophy"
            },
            {
                "id": "DOID:0060455",
                "name": "anterior limiting membrane dystrophy type II"
            },
            {
                "id": "DOID:0060455",
                "name": "corneal dystrophy honeycomb-shaped"
            },
            {
                "id": "DOID:0060455",
                "name": "corneal dystrophy of Bowman layer type II"
            },
            {
                "id": "MONDO:0011185",
                "name": "Thiel-Behnke corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "TBCD"
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            {
                "id": "MONDO:0011185",
                "name": "Thiel-Behnke corneal dystrophy"
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            {
                "id": "MONDO:0011185",
                "name": "Waardenburg-Jonker corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "anterior limiting membrane dystrophy type 2"
            },
            {
                "id": "MONDO:0011185",
                "name": "anterior limiting membrane dystrophy type II"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy of Bowman layer type 2"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy of Bowman layer type II"
            },
            {
                "id": "MONDO:0011185",
                "name": "curly fiber corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "curly fibre corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "honeycomb corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "CDB2"
            },
            {
                "id": "MONDO:0011185",
                "name": "CDTB"
            },
            {
                "id": "MONDO:0011185",
                "name": "Thiel Behnke corneal dystrophy"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy Thiel Behnke type"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy honeycomb shaped"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy of the Bowman layer type 2"
            },
            {
                "id": "MONDO:0011185",
                "name": "corneal dystrophy, Thiel-Behnke type"
            },
            {
                "id": "MIM:602082",
                "name": "Corneal dystrophy, Thiel-Behnke type"
            }
        ],
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        "record_type": "disease"
    },
    {
        "record_id": "doid.0060456",
        "disease_id": "DOID:0060456",
        "recommended_name": "Schnyder corneal dystrophy",
        "synonyms": [
            {
                "id": "DOID:0060456",
                "name": "SCCD"
            },
            {
                "id": "DOID:0060456",
                "name": "Schnyder crystalline corneal dystrophy"
            },
            {
                "id": "DOID:0060456",
                "name": "corneal dystrophy crystalline of Schnyder"
            },
            {
                "id": "DOID:0060456",
                "name": "crystalline stromal dystrophy"
            },
            {
                "id": "DOID:0060456",
                "name": "hereditary crystalline stromal dystrophy of Schnyder"
            },
            {
                "id": "MONDO:0007374",
                "name": "Schnyder corneal dystrophy"
            },
            {
                "id": "MONDO:0007374",
                "name": "SCCD"
            },
            {
                "id": "MONDO:0007374",
                "name": "SCD"
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                "id": "MONDO:0007374",
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            {
                "id": "MONDO:0011485",
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            {
                "id": "MIM:604777",
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                "id": "DOID:0060720",
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                "id": "DOID:0060720",
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                "id": "MONDO:0009183",
                "name": "epidermolysis bullosa junctionalis with pyloric atresia"
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                "id": "MONDO:0009183",
                "name": "epidermolysis bullosa, junctional, with pyloric stenosis"
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                "name": "junctional epidermolysis bullosa with pyloric atresia"
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                "id": "MONDO:0009183",
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                "id": "DOID:0060735",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
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                "id": "MONDO:0007550",
                "name": "epidermolysis bullosa simplex, generalised severe"
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                "id": "MIM:131760",
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                "id": "DOID:0060736",
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                "id": "DOID:0060736",
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                "id": "DOID:0060736",
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                "id": "MONDO:0007555",
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                "id": "DOID:0060737",
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                "id": "DOID:0060737",
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                "id": "DOID:0060737",
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                "id": "DOID:0060737",
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                "id": "MONDO:0009182",
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                "id": "MONDO:0009182",
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                "id": "MONDO:0009182",
                "name": "JEB, generalized severe"
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                "id": "DOID:0060738",
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            {
                "id": "MONDO:0007471",
                "name": "Doyne honeycomb retinal dystrophy"
            },
            {
                "id": "MONDO:0007471",
                "name": "Malattia leventinese"
            },
            {
                "id": "MONDO:0007471",
                "name": "dominant drusen"
            },
            {
                "id": "MONDO:0007471",
                "name": "dominant radial drusen"
            },
            {
                "id": "MONDO:0007471",
                "name": "DHD"
            },
            {
                "id": "MIM:126600",
                "name": "Doyne honeycomb retinal dystrophy"
            }
        ],
        "record_url": "http://disease-ontology.org/term/DOID:0060745",
        "snv_count": 0,
        "protein_count": 5,
        "glycan_count": 0,
        "biomarker_count": 0,
        "species_list": "Zebrafish;Mouse;Human;Rat",
        "biomarker_type": "",
        "biomarker_id": "",
        "hit_score": 0.6,
        "record_type": "disease"
    },
    {
        "record_id": "doid.0060746",
        "disease_id": "DOID:0060746",
        "recommended_name": "basal laminar drusen",
        "synonyms": [
            {
                "id": "DOID:0060746",
                "name": "cuticular drusen"
            },
            {
                "id": "DOID:0060746",
                "name": "drusen of bruch membrane"
            },
            {
                "id": "DOID:0060746",
                "name": "early adult-onset grouped drusen"
            },
            {
                "id": "MONDO:0007472",
                "name": "basal laminar drusen"
            },
            {
                "id": "MONDO:0007472",
                "name": "basal laminar drusen"
            },
            {
                "id": "MONDO:0007472",
                "name": "drusen of Bruch membrane"
            },
            {
                "id": "MIM:126700",
                "name": "Basal laminar drusen"
            }
        ],
        "record_url": "http://disease-ontology.org/term/DOID:0060746",
        "snv_count": 0,
        "protein_count": 5,
        "glycan_count": 0,
        "biomarker_count": 0,
        "species_list": "Zebrafish;Mouse;Human;Rat",
        "biomarker_type": "",
        "biomarker_id": "",
        "hit_score": 0.6,
        "record_type": "disease"
    }
]
