{
    "disease_id": "DOID:0080206", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "congenital anomalies of kidney and urinary tract 1, susceptibility to"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "renal hypodysplasia, nonsyndromic, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "congenital anomaly of kidney and urinary tract caused by mutation in DSTYK"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "congenital anomalies of kidney and urinary tract 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "congenital anomalies of kidney and urinary tract 1, susceptibility to; CAKUT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "congenital anomalies of kidney and urinary tract 1; CAKUT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012561", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012561", 
            "name": "DSTYK congenital anomaly of kidney and urinary tract"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080206", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080206", 
            "name": "Congenital anomalies of the kidney and urinary tract 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080206", 
        "description": "A CAKUT that has_material_ basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080206", 
        "name": "CAKUT1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080206#disease-associations", 
            "id": "0080206", 
            "database": "Alliance of Genome Resources"
        }
    ]
}