{
    "disease_id": "DOID:14692",
    "recommended_name": {
        "id": "DOID:14692",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14692",
        "name": "Smith-Lemli-Opitz syndrome",
        "description": ""
    },
    "synonyms": [
        {
            "id": "DOID:14692",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14692",
            "name": "Smith-Opitz-Inborn syndrome",
            "description": ""
        },
        {
            "id": "DOID:14692",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14692",
            "name": "Rutledge lethal multiple congenital anomaly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Smith-Lemli-Opitz syndrome",
            "description": "Smith-Lemli-Opitz syndrome (SLOS) is characterized by multiple congenital anomalies, intellectual deficit, and behavioral problems."
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "polydactyly, sex reversal, renal hypoplasia, and unilobular lung",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Smith Lemli Opitz syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "lethal acrodysgenital syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Smith-Lemli-Opitz syndrome; SLOS",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "7-dehydrocholesterol reductase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Rutledge lethal multiple congenital anomaly syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "SLO syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "RSH syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "SLOS",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Smith-Opitz-inborn syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "polydactyly, sex reversal, renal hypoplasia, and unilobar lung",
            "description": ""
        },
        {
            "id": "MONDO:0010035",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010035",
            "name": "Smith-Lemli-Opitz syndrome",
            "description": ""
        },
        {
            "id": "MIM:270400",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/270400",
            "name": "Smith-Lemli-Opitz syndrome",
            "description": "Smith-Lemli-Opitz syndrome"
        }
    ]
}