{
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            "description": "", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009758", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009758", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009758", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009758", 
            "name": "congenital stationary night blindness 1B autosomal recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009758", 
            "name": "congenital stationary night blindness type 1B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009758", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009758", 
            "name": "autosomal recessive complete congenital stationary night blindness"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110865", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110865", 
            "name": "CSNB1B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110865", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110865", 
            "name": "congenital stationary night blindness 1B autosomal recessive"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110865", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110865", 
            "name": "autosomal recessive complete congenital stationary night blindness"
        }, 
        {
            "url": "https://www.omim.org/entry/257270", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:257270", 
            "name": "Night blindness, congenital stationary, 1B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110865", 
        "description": "A congenital stationary night blindness characterized by autosomal recessive inheritance that has_material_basis_in mutation in the GRM6 gene on chromosome 5q35.", 
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    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/257270", 
            "id": "257270", 
            "database": "MIM"
        }
    ]
}