{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "OCRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "oculocerebrorenal syndrome of Lowe"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Lowe syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Lowe oculocerebrorenal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "oculocerebrorenal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "OCR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Lowe disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "oculo-cerebro-renal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "oculo-cerebro-renal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Lowe oculo-cerebro-renal syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Lowe oculocerebrorenal syndrome; OCRL"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010645", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010645", 
            "name": "Ocrl1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1056", 
            "name": "Lowe syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1056", 
            "name": "lowe oculocerebrorenal syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:1056", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1056", 
            "name": "oculocerebrorenal syndrome of Lowe"
        }, 
        {
            "url": "https://www.omim.org/entry/309000", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:309000", 
            "name": "Lowe oculocerebrorenal syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1056", 
        "description": "A syndrome that has_material_basis_in mutation in the OCRL gene on chromosome Xq26 and that is characterized by hydrophthalmia, cataract, mental retardation, vitamin D-resistant rickets, amino aciduria, and reduced ammonia production by the kidney.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1056", 
        "name": "oculocerebrorenal syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/309000", 
            "id": "309000", 
            "database": "MIM"
        }
    ]
}