{
    "disease_id": "DOID:0111809",
    "recommended_name": {
        "id": "DOID:0111809",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0111809",
        "name": "syndromic microphthalmia 2",
        "description": "A syndromic microphthalmia characterized by ocular defects including microphthalmia, microcornea, and congentital cataract; facial dysmorphism including septate nasal cartilage with high nasal bridge; congenital heart defects, most commonly a septal defect; and dental anomalies, most commonly persistent primary teeth and radiculomegaly that has_material_basis_in mutation in the BCL6 corepressor gene on chromosome Xp11."
    },
    "synonyms": [
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "ANOP2",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "MAA2",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "MCOPS2",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "OFCD syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "oculofaciocardiodental syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "syndromic microphthalmia type 2",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome",
            "description": ""
        },
        {
            "id": "DOID:0111809",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0111809",
            "name": "microphthalmia cataracts radiculomegaly and septal heart defects",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia, syndromic 2",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "OFCD syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia syndromic 2",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia, syndromic 2",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia, syndromic 2, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia, syndromic type 2",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "oculofaciocardiodental syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "ANOP2 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "MAA2 (formerly)",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "MCOPS2",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "microphthalmia cataracts radiculomegaly and septal heart defects",
            "description": ""
        },
        {
            "id": "MONDO:0010261",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010261",
            "name": "syndromic microphthalmia type 2",
            "description": ""
        },
        {
            "id": "MIM:300166",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300166",
            "name": "Microphthalmia, syndromic, 2",
            "description": "Microphthalmia, syndromic, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111809"
    ],
    "unlinked_id_list": []
}