{
    "disease_id": "DOID:14291",
    "recommended_name": {
        "id": "DOID:14291",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:14291",
        "name": "Noonan syndrome with multiple lentigines",
        "description": "A RASopathy that is characterized by autosomal dominant inheritance of brown skin spots called lentigines that are similar to freckles, heart defects, widely spaced eyes a sunken chest or protruding chest  and short stature."
    },
    "synonyms": [
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "LEOPARD syndrome",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Generalized lentiginosis",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Gorlin syndrome II",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Lentiginosis profusa syndrome",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Moynahan syndrome",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Multiple lentigines syndrome",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Progressive cardiomyopathic lentiginosis",
            "description": ""
        },
        {
            "id": "DOID:14291",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:14291",
            "name": "Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "Noonan syndrome with multiple lentigines",
            "description": "Noonan syndrome with multiple lentigines (NSML), previously known as LEOPARD syndrome, is a rare multisystem genetic disorder characterized by lentigines, hypertrophic cardiomyopathy, short stature, pectus deformity, and dysmorphic facial features."
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "progressive cardiomyopathic lentiginosis",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "generalized lentiginosis",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "lentiginosis profusa syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "LPRD1",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "Gorlin syndrome II",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "Moynahan syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "LEOPARD syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "Cardiomyopathic lentiginosis",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "LEOPARD syndrome 1",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "multiple lentigines syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "familial multiple lentigines syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "cardiocutaneous syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "LEOPARD syndrome 1; LPRD1",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "LEOPARD syndrome type 1",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007893",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007893",
            "name": "lentiginosis, Cardiomyopathic",
            "description": ""
        },
        {
            "id": "MIM:151100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/151100",
            "name": "LEOPARD syndrome 1",
            "description": "LEOPARD syndrome 1"
        }
    ]
}