{
    "disease_id": "DOID:0111334", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013991", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013991", 
            "name": "obesity due to congenital leptin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013991", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013991", 
            "name": "LEPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013991", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013991", 
            "name": "leptin deficiency or dysfunction"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013991", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013991", 
            "name": "leptin deficiency or dysfunction; LEPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013991", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013991", 
            "name": "obesity, morbid, nonsyndromic 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111334", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111334", 
            "name": "LEPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111334", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111334", 
            "name": "leptin deficiency or dysfunction"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111334", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111334", 
            "name": "morbid obesity"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111334", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111334", 
            "name": "obesity due to congenital leptin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111334", 
        "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.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111334", 
        "name": "congenital leptin deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111334#disease-associations", 
            "id": "0111334", 
            "database": "Alliance of Genome Resources"
        }
    ]
}