{
    "disease_id": "DOID:0111798", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "nephrolithiasis, X-linked recessive, with renal failure"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "urolithiasis, X-linked recessive, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "XRN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "nephrolithiasis, X-linked recessive, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "nephrolithiasis 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010687", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010687", 
            "name": "nephrolithiasis, X-linked recessive, with renal failure; XRN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "NPHL1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "XRN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "X-linked nephrolithiasis with renal failure"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "X-linked recessive urolithiasis type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "nephrolithiasis 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111798", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111798", 
            "name": "nephrolithiasis X-linked recessive type 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111798", 
        "description": "A renal tubular transport disease characterized by proximal renal tubular reabsorptive failure, hypercalciuria, nephrolithiasis, and renal insufficiency with absence of rickets that has_material_basis_in hemizygous or homozygous mutation in CLCN5 on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111798", 
        "name": "X-linked nephrolithiasis type I"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111798#disease-associations", 
            "id": "0111798", 
            "database": "Alliance of Genome Resources"
        }
    ]
}