{
    "disease_id": "DOID:0111800", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "microphthalmia, syndromic 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "RARB syndromic microphthalmia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "microphthalmia, syndromic type 12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or Cardiac defects"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "MCOPS12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "microphthalmia, syndromic 12; MCOPS12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "syndromic microphthalmia-12"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014229", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014229", 
            "name": "syndromic microphthalmia caused by mutation in RARB"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111800", 
            "name": "MCOPS12"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111800", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111800", 
            "name": "microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or cardiac defects"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111800", 
        "description": "A syndromic microphthalmia characterized by bilateral microphthalmia, pulmonary hypoplasia, and diaphragmatic hernia that has_material_basis_in compound heterozygous or heterozygous mutation in RARB on chromosome 3p24.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111800", 
        "name": "syndromic microphthalmia 12"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111800#disease-associations", 
            "id": "0111800", 
            "database": "Alliance of Genome Resources"
        }
    ]
}