{
    "disease_id": "DOID:1930", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:1930", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:1930", 
            "name": "LNMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009514", 
            "description": "Laurence-Moon syndrome (LMS) is a very rare genetic multisystemic disorder characterized by pituitary dysfunction, ataxia, peripheral neuropathy, spastic paraplegia, and chorioretinal dystrophy.", 
            "resource": "MONDO", 
            "id": "MONDO:0009514", 
            "name": "Laurence-Moon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009514", 
            "name": "Laurence-Moon syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009514", 
            "name": "Laurence-MOON syndrome; LNMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009514", 
            "name": "LNMS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009514", 
            "name": "Laurence-Moon-Biedl syndrome"
        }, 
        {
            "url": "https://www.omim.org/entry/245800", 
            "description": "Laurence-Moon syndrome", 
            "resource": "MIM", 
            "id": "MIM:245800", 
            "name": "Laurence-Moon syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:1930", 
        "description": "A syndrome characterized by pituitary dysfunction, childhood onset ataxia, peripheral neuropathy, spastic paraplegia, and chorioretinopathy that has_material_basis_in homozygous or compound heterozygous mutation in PNPLA6 on chromosome 19p13.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:1930", 
        "name": "Laurence-Moon syndrome"
    }
}