{
    "disease_id": "DOID:14692", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "polydactyly, sex reversal, renal hypoplasia, and unilobular lung"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "Smith Lemli Opitz syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "lethal acrodysgenital syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "Smith-Lemli-Opitz syndrome; SLOS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "7-dehydrocholesterol reductase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "Rutledge lethal multiple congenital anomaly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "SLO syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "RSH syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "SLOS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "Smith-Opitz-inborn syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010035", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010035", 
            "name": "polydactyly, sex reversal, renal hypoplasia, and unilobar lung"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14692", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14692", 
            "name": "Smith-Opitz-Inborn syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14692", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14692", 
            "name": "Rutledge lethal multiple congenital anomaly syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14692", 
        "description": "", 
        "resource": "Disease Ontology", 
        "id": "DOID:14692", 
        "name": "Smith-Lemli-Opitz syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14692#disease-associations", 
            "id": "14692", 
            "database": "Alliance of Genome Resources"
        }
    ]
}