{
    "disease_id": "DOID:0111620", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "corneal dystrophy and sensorineural deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "corneal dystrophy and perceptive deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "corneal dystrophy and perceptive deafness; CDPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "corneal dystrophy with progressive deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "Cdpd1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "CDPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "Harboyan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009015", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009015", 
            "name": "congenital corneal dystrophy, progressive sensorineural deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "CDPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "CDPD1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "Harboyan syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "corneal endothelial dystrophy and perceptive deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "corneal dystrophy and perceptive deafness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111620", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111620", 
            "name": "corneal dystrophy with progressive deafness"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111620", 
        "description": "A syndrome characterized by congenital corneal endothelial dystrophy and progressive, postlingual sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in SLC4A11 on chromosome 20p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111620", 
        "name": "corneal dystrophy-perceptive deafness syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111620#disease-associations", 
            "id": "0111620", 
            "database": "Alliance of Genome Resources"
        }
    ]
}