{
    "disease_id": "DOID:0111799", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "microphthalmia, syndromic 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "Maa"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "Lenz microphthalmia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "microphthalmia, syndromic 1; MCOPS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "Lenz dysplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "microphthalmia, syndromic type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "MCOPS1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010671", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010671", 
            "name": "Maa, formerly"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111799", 
            "name": "Lenz dysplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111799", 
            "name": "MCOPS1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111799", 
            "name": "Lenz microphthalmia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111799", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111799", 
            "name": "Lenz type microphthalmia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111799", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111799", 
        "name": "syndromic microphthalmia 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111799#disease-associations", 
            "id": "0111799", 
            "database": "Alliance of Genome Resources"
        }
    ]
}