{
    "disease_id": "DOID:0111544", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008301", 
            "name": "preaxial deficiency, postaxial polydactyly, and hypospadias"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008301", 
            "name": "autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008301", 
            "name": "preaxial deficiency-postaxial polydactyly-hypospadias syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008301", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008301", 
            "name": "preaxial deficiency, postaxial polydactyly and hypospadias"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111544", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111544", 
            "name": "preaxial deficiency-postaxial polydactyly-hypospadias syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111544", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111544", 
            "name": "autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111544", 
        "description": "A syndrome characterized by preaxial deficiencies of the hands and feet, postaxial polydactyly of the hands, and hypospadias that has_material_basis_in heterozygous mutation in HOXA13 on chromosome 7p15.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111544", 
        "name": "Guttmacher syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/176305", 
            "id": "176305", 
            "database": "MIM"
        }
    ]
}