{
    "disease_id": "DOID:0111334",
    "recommended_name": {
        "id": "DOID:0111334",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0111334",
        "name": "congenital leptin deficiency",
        "description": "A syndrome characterized by severe early-onset obesity, hyperphagia, hypogonadotropic hypogonadism, and neuroendocrine and metabolic dysfunction that has_material_basis_in homozygous or compound heterozygous mutation in LEP on chromosome 7q32.1."
    },
    "synonyms": [
        {
            "id": "DOID:0111334",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111334",
            "name": "LEPD",
            "description": ""
        },
        {
            "id": "DOID:0111334",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111334",
            "name": "leptin deficiency or dysfunction",
            "description": ""
        },
        {
            "id": "DOID:0111334",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0111334",
            "name": "obesity due to congenital leptin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "obesity due to congenital leptin deficiency",
            "description": "Congenital leptin deficiency is a form of monogenic obesity characterized by severe early-onset obesity and marked hyperphagia."
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "Congenital Leptin Deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "obesity, morbid, due to leptin deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "LEPD",
            "description": ""
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "leptin deficiency or dysfunction",
            "description": ""
        },
        {
            "id": "MONDO:0013991",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013991",
            "name": "obesity, morbid, nonsyndromic 1",
            "description": ""
        },
        {
            "id": "MIM:614962",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614962",
            "name": "Leptin deficiency",
            "description": "Leptin deficiency"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0111334"
    ],
    "unlinked_id_list": []
}