{
    "disease_id": "DOID:0080207", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "congenital anomalies of kidney and urinary tract type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "congenital anomaly of kidney and urinary tract caused by mutation in TBX18"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "ureteropelvic junction obstruction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "hydronephrosis due to Pujo"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "congenital anomalies of kidney and urinary tract 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "multicystic renal dysplasia, bilateral"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "congenital anomalies of kidney and urinary tract 2; CAKUT2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "pelviureteric junction obstruction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0027676", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0027676", 
            "name": "TBX18 congenital anomaly of kidney and urinary tract"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080207", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080207", 
            "name": "Congenital anomalies of the kidney and urinary tract 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080207", 
        "description": "A CAKUT that has_material_basis_in heterozygous mutation in the TBX18 gene on chromosome 6q14.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080207", 
        "name": "CAKUT2"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080207#disease-associations", 
            "id": "0080207", 
            "database": "Alliance of Genome Resources"
        }
    ]
}