{
    "disease_id": "DOID:0080661", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "aplasia cutis congenita (disease)"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "aplasia cutis congenita, nonsyndromic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "scalp defect congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "aplasia cutis congenita nonsyndromic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "scalp defect, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "congenital defect of skull and scalp"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "aplasia cutis congenita"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "aplasia cutis congenita, nonsyndromic; ACC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007145", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007145", 
            "name": "ACC"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080661", 
        "description": "A skin disease characterized by localized areas of missing skin that resemble ulcers or oopen wounds in new borns and that has_material_basis_in  heterozygous mutation in the BMS1 gene on chromosome 10q11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080661", 
        "name": "nonsyndromic aplasia cutis congenita"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080661#disease-associations", 
            "id": "0080661", 
            "database": "Alliance of Genome Resources"
        }
    ]
}