{
    "disease_id": "DOID:0080548", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "Noonan syndrome with multiple lentigines"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "progressive cardiomyopathic lentiginosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "generalized lentiginosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "lentiginosis profusa syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "LPRD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "Gorlin syndrome II"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "Moynahan syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "LEOPARD syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "Cardiomyopathic lentiginosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "LEOPARD syndrome 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "multiple lentigines syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "familial multiple lentigines syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "cardiocutaneous syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "LEOPARD syndrome 1; LPRD1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "LEOPARD syndrome type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007893", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007893", 
            "name": "lentiginosis, Cardiomyopathic"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0080548", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0080548", 
            "name": "LEOPARD syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080548", 
        "description": "A Noonan syndrome with multiple lentigines that has_material_basis_in heterozygous mutation in the PTPN11 gene on chromosome 12q24.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080548", 
        "name": "Noonan syndrome with multiple lentigines 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080548#disease-associations", 
            "id": "0080548", 
            "database": "Alliance of Genome Resources"
        }
    ]
}