{
    "disease_id": "DOID:11830",
    "recommended_name": {
        "id": "DOID:11830",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:11830",
        "name": "myopia",
        "description": "A refractive error characterized by the inability to see farther objects clearly."
    },
    "synonyms": [
        {
            "id": "DOID:11830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11830",
            "name": "near vision",
            "description": ""
        },
        {
            "id": "DOID:11830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11830",
            "name": "near-sightedness",
            "description": ""
        },
        {
            "id": "DOID:11830",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:11830",
            "name": "short-sightedness",
            "description": ""
        },
        {
            "id": "MONDO:0012389",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012389",
            "name": "MYP12",
            "description": ""
        },
        {
            "id": "MONDO:0012389",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012389",
            "name": "MYP12",
            "description": ""
        },
        {
            "id": "MONDO:0012389",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012389",
            "name": "myopia 12, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012389",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012389",
            "name": "myopia 12, autosomal dominant; MYP12",
            "description": ""
        },
        {
            "id": "MONDO:0012229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012229",
            "name": "MYP9",
            "description": ""
        },
        {
            "id": "MONDO:0012229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012229",
            "name": "myopia 9",
            "description": ""
        },
        {
            "id": "MONDO:0012229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012229",
            "name": "myopia 9; MYP9",
            "description": ""
        },
        {
            "id": "MONDO:0012229",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012229",
            "name": "MYP9",
            "description": ""
        },
        {
            "id": "MONDO:0012230",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012230",
            "name": "MYP10",
            "description": ""
        },
        {
            "id": "MONDO:0012230",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012230",
            "name": "myopia 10",
            "description": ""
        },
        {
            "id": "MONDO:0012230",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012230",
            "name": "myopia 10; MYP10",
            "description": ""
        },
        {
            "id": "MONDO:0012230",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012230",
            "name": "MYP10",
            "description": ""
        },
        {
            "id": "MONDO:0012227",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012227",
            "name": "MYP7",
            "description": ""
        },
        {
            "id": "MONDO:0012227",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012227",
            "name": "myopia 7",
            "description": ""
        },
        {
            "id": "MONDO:0012227",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012227",
            "name": "myopia 7; MYP7",
            "description": ""
        },
        {
            "id": "MONDO:0012227",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012227",
            "name": "MYP7",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "schizophrenia 16",
            "description": "A schizophrenia that has_material_basis_in a mutation on chromosome 7q36.3."
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "schizophrenia 16; SCZD16",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "chromosome 7Q36.3 Duplication syndrome, 362-Kb",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "schizophrenia susceptibility locus, chromosome 7Q36.3-related",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "SCZD16",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "schizophrenia 16",
            "description": ""
        },
        {
            "id": "MONDO:0013506",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013506",
            "name": "schizophrenia type 16",
            "description": ""
        },
        {
            "id": "MONDO:0010685",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010685",
            "name": "MYP1",
            "description": ""
        },
        {
            "id": "MONDO:0010685",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010685",
            "name": "MYP1",
            "description": ""
        },
        {
            "id": "MONDO:0010685",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010685",
            "name": "myopia 1, X-linked; MYP1",
            "description": ""
        },
        {
            "id": "MONDO:0010685",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010685",
            "name": "myopia 1, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010377",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010377",
            "name": "MYP13",
            "description": ""
        },
        {
            "id": "MONDO:0010377",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010377",
            "name": "myopia 13, X-linked",
            "description": ""
        },
        {
            "id": "MONDO:0010377",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010377",
            "name": "MYP13",
            "description": ""
        },
        {
            "id": "MONDO:0010377",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010377",
            "name": "myopia 13, X-linked; MYP13",
            "description": ""
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "myopia 21, autosomal dominant",
            "description": "Any myopia (disease) in which the cause of the disease is a mutation in the ZNF644 gene."
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "ZNF644 myopia (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "myopia (disease) caused by mutation in ZNF644",
            "description": ""
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "myopia 21, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "myopia 21, autosomal dominant; MYP21",
            "description": ""
        },
        {
            "id": "MONDO:0013604",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013604",
            "name": "MYP21",
            "description": ""
        },
        {
            "id": "MONDO:0012932",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012932",
            "name": "MYP16",
            "description": ""
        },
        {
            "id": "MONDO:0012932",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012932",
            "name": "myopia 16, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012932",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012932",
            "name": "myopia 16, autosomal dominant; MYP16",
            "description": ""
        },
        {
            "id": "MONDO:0012932",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012932",
            "name": "MYP16",
            "description": ""
        },
        {
            "id": "MONDO:0014177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014177",
            "name": "myopia 22, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014177",
            "name": "myopia 22, autosomal dominant; MYP22",
            "description": ""
        },
        {
            "id": "MONDO:0014177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014177",
            "name": "myopia 22, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014177",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014177",
            "name": "MYP22",
            "description": ""
        },
        {
            "id": "MONDO:0014411",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014411",
            "name": "myopia 24, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014411",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014411",
            "name": "myopia 24, autosomal dominant; MYP24",
            "description": ""
        },
        {
            "id": "MONDO:0014411",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014411",
            "name": "myopia 24, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0014411",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014411",
            "name": "MYP24",
            "description": ""
        },
        {
            "id": "MONDO:0012228",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012228",
            "name": "MYP8",
            "description": ""
        },
        {
            "id": "MONDO:0012228",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012228",
            "name": "myopia 8",
            "description": ""
        },
        {
            "id": "MONDO:0012228",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012228",
            "name": "myopia 8; MYP8",
            "description": ""
        },
        {
            "id": "MONDO:0012228",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012228",
            "name": "MYP8",
            "description": ""
        },
        {
            "id": "MONDO:0009713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009713",
            "name": "MYP18",
            "description": ""
        },
        {
            "id": "MONDO:0009713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009713",
            "name": "myopia 18, autosomal recessive; MYP18",
            "description": ""
        },
        {
            "id": "MONDO:0009713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009713",
            "name": "MYP18",
            "description": ""
        },
        {
            "id": "MONDO:0009713",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009713",
            "name": "myopia 18, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014183",
            "name": "myopia 23, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0014183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014183",
            "name": "MYP23",
            "description": ""
        },
        {
            "id": "MONDO:0014183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014183",
            "name": "myopia 23, autosomal recessive; MYP23",
            "description": ""
        },
        {
            "id": "MONDO:0014183",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014183",
            "name": "myopia 23, autosomal recessive",
            "description": ""
        },
        {
            "id": "MONDO:0011300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011300",
            "name": "MYP3",
            "description": ""
        },
        {
            "id": "MONDO:0011300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011300",
            "name": "MYP3",
            "description": ""
        },
        {
            "id": "MONDO:0011300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011300",
            "name": "myopia 3, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0011300",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011300",
            "name": "myopia 3, autosomal dominant; MYP3",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia 6",
            "description": "Any myopia in which the cause of the disease is a mutation in the SCO2 gene."
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia, susceptibility to",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "MYP6",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia 6",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "SCO2 myopia (disease)",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia type 6",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia 6; MYP6",
            "description": ""
        },
        {
            "id": "MONDO:0012154",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012154",
            "name": "myopia (disease) caused by mutation in SCO2",
            "description": ""
        },
        {
            "id": "MONDO:0012388",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012388",
            "name": "MYP11",
            "description": ""
        },
        {
            "id": "MONDO:0012388",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012388",
            "name": "MYP11",
            "description": ""
        },
        {
            "id": "MONDO:0012388",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012388",
            "name": "myopia 11, autosomal dominant; MYP11",
            "description": ""
        },
        {
            "id": "MONDO:0012388",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012388",
            "name": "myopia 11, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012995",
            "name": "MYP15",
            "description": ""
        },
        {
            "id": "MONDO:0012995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012995",
            "name": "myopia 15, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012995",
            "name": "myopia 15, autosomal dominant; MYP15",
            "description": ""
        },
        {
            "id": "MONDO:0012995",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012995",
            "name": "MYP15",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "MYP17",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "myopia 17, autosomal dominant; MYP17",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "myopia 4, formerly",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "MYP17",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "myopia 4",
            "description": ""
        },
        {
            "id": "MONDO:0012021",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012021",
            "name": "myopia 17, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012469",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012469",
            "name": "MYP14",
            "description": ""
        },
        {
            "id": "MONDO:0012469",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012469",
            "name": "MYP14",
            "description": ""
        },
        {
            "id": "MONDO:0012469",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012469",
            "name": "myopia 14; MYP14",
            "description": ""
        },
        {
            "id": "MONDO:0012469",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012469",
            "name": "myopia 14",
            "description": ""
        },
        {
            "id": "MONDO:0012045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012045",
            "name": "MYP5",
            "description": ""
        },
        {
            "id": "MONDO:0012045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012045",
            "name": "myopia 5, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0012045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012045",
            "name": "myopia 5, autosomal dominant; MYP5",
            "description": ""
        },
        {
            "id": "MONDO:0012045",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012045",
            "name": "MYP5",
            "description": ""
        },
        {
            "id": "MONDO:0008053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008053",
            "name": "MYP2",
            "description": ""
        },
        {
            "id": "MONDO:0008053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008053",
            "name": "myopia 2, autosomal dominant; MYP2",
            "description": ""
        },
        {
            "id": "MONDO:0008053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008053",
            "name": "MYP2",
            "description": ""
        },
        {
            "id": "MONDO:0008053",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008053",
            "name": "myopia 2, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013508",
            "name": "MYP19",
            "description": ""
        },
        {
            "id": "MONDO:0013508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013508",
            "name": "myopia 19, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013508",
            "name": "myopia 19, autosomal dominant; MYP19",
            "description": ""
        },
        {
            "id": "MONDO:0013508",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013508",
            "name": "MYP19",
            "description": ""
        },
        {
            "id": "MONDO:0013603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013603",
            "name": "MYP20",
            "description": ""
        },
        {
            "id": "MONDO:0013603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013603",
            "name": "myopia 20, autosomal dominant",
            "description": ""
        },
        {
            "id": "MONDO:0013603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013603",
            "name": "MYP20",
            "description": ""
        },
        {
            "id": "MONDO:0013603",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013603",
            "name": "myopia 20, autosomal dominant; MYP20",
            "description": ""
        },
        {
            "id": "MIM:614167",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614167",
            "name": "Myopia 21, autosomal dominant",
            "description": "Myopia 21, autosomal dominant"
        },
        {
            "id": "MIM:615420",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615420",
            "name": "Myopia 22, autosomal dominant",
            "description": "Myopia 22, autosomal dominant"
        },
        {
            "id": "MIM:615946",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615946",
            "name": "Myopia 24, autosomal dominant",
            "description": "Myopia 24, autosomal dominant"
        },
        {
            "id": "MIM:615431",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615431",
            "name": "Myopia 23, autosomal recessive",
            "description": "Myopia 23, autosomal recessive"
        },
        {
            "id": "MIM:608908",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/608908",
            "name": "Myopia 6",
            "description": "Myopia 6"
        }
    ]
}