{
    "disease_id": "DOID:0111255", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "MKKS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "hydrometrocolpos, postaxial polydactyly, and congenital heart malformation"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "Kaufman-Mckusick syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "MCKUSICK-Kaufman syndrome; MKKS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "Kaufman McKusick syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "HMCS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "hydrometrocolpos-postaxial polydactyly syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "hydrometrocolpos syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009367", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009367", 
            "name": "McKusick Kaufman syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "HMCS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "hydrometrocolpos, postaxial polydactyly, and congenital heart malformation"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "Kaufman McKusick syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "MKKS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "hydrometrocolpos syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111255", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111255", 
            "name": "hydrometrocolpos-postaxial polydactyly syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111255", 
        "description": "A syndrome characterized by neonatal onset of genitourinary malformations, especially hydrometrocolpos, polydactyly, and, more rarely, heart or gastrointestinal malformations that has_material_basis_in homozygous or compound heterozygous mutation in MKKS on 20p12.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111255", 
        "name": "McKusick-Kaufman syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111255#disease-associations", 
            "id": "0111255", 
            "database": "Alliance of Genome Resources"
        }
    ]
}