{
    "disease_id": "DOID:0111531", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "isolated optic nerve hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "optic nerve hypoplasia, familial bilateral"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "familial bilateral optic nerve hypoplasia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "optic nerve aplasia, bilateral"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "optic nerve hypoplasia, bilateral"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008136", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008136", 
            "name": "isolated optic nerve hypoplasia/aplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111531", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111531", 
            "name": "ONH"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111531", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111531", 
            "name": "familial bilateral optic nerve hypoplasia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111531", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111531", 
            "name": "isolated optic nerve hypoplasia/aplasia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111531", 
        "description": "An optic nerve disease characterized by isolated optic nerve hypoplasia or aplasia that has_material_basis_in heterozygous mutation in PAX6 on chromosome 11p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111531", 
        "name": "bilateral optic nerve hypoplasia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/165550", 
            "id": "165550", 
            "database": "MIM"
        }
    ]
}