{
    "disease_id": "DOID:0060599", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "cataract-dental syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "Nance-Horan syndrome; NHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "cataract X-linked with Hutchinsonian teeth"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "Mesiodens cataract syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "cataract, X-linked, with Hutchinsonian teeth"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "cataract dental syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "NHS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010545", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010545", 
            "name": "Mesiodens-cataract syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060599", 
        "description": "A syndrome that has_material_basis_in mutation in the NHS gene on chromosome Xp22 and is characterized by congenital cataract leading to profound vision loss, characteristic dysmorphic features and dental anomalies.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060599", 
        "name": "Nance-Horan syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/302350", 
            "id": "302350", 
            "database": "MIM"
        }
    ]
}