{
    "disease_id": "DOID:0111799",
    "recommended_name": {
        "id": "DOID:0111799",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111799",
        "name": "syndromic microphthalmia 1",
        "description": "A syndromic microphthalmia characterized by unilateral or bilateral microphthalmia or anophthalmia and defects in the skeletal and genitourinary system that has_material_basis_in mutation in NAA10 on chromosome Xq28."
    },
    "synonyms": [
        {
            "id": "DOID:0111799",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111799",
            "name": "Lenz dysplasia",
            "description": ""
        },
        {
            "id": "DOID:0111799",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111799",
            "name": "MCOPS1",
            "description": ""
        },
        {
            "id": "DOID:0111799",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111799",
            "name": "Lenz microphthalmia",
            "description": ""
        },
        {
            "id": "DOID:0111799",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111799",
            "name": "Lenz type microphthalmia",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "microphthalmia, syndromic 1",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "Maa",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "Lenz microphthalmia syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "microphthalmia, syndromic 1; MCOPS1",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "Lenz dysplasia",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "microphthalmia, syndromic type 1",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "microphthalmia, syndromic 1",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "MCOPS1",
            "description": ""
        },
        {
            "id": "MONDO:0010671",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010671",
            "name": "Maa, formerly",
            "description": ""
        },
        {
            "id": "MIM:309800",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/309800",
            "name": "Microphthalmia, syndromic, 1",
            "description": "Microphthalmia, syndromic, 1"
        }
    ]
}