{
    "disease_id": "DOID:0060599",
    "recommended_name": {
        "id": "DOID:0060599",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0060599",
        "name": "Nance-Horan syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "Nance-Horan syndrome",
            "description": "A syndrome characterized by the association in male patients of congenital cataracts with microcornea, dental anomalies and facial dysmorphism."
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "Nance-Horan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "nance-horan syndrome, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "Mesiodens cataract syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "NHS",
            "description": ""
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "cataract X-linked with Hutchinsonian teeth",
            "description": ""
        },
        {
            "id": "MONDO:0010545",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010545",
            "name": "cataract dental syndrome",
            "description": ""
        },
        {
            "id": "MIM:302350",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/302350",
            "name": "Nance-Horan syndrome",
            "description": "Nance-Horan syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0060599"
    ],
    "unlinked_id_list": []
}