{
    "disease_id": "DOID:0111698", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010961", 
            "name": "obesity due to prohormone convertase i deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010961", 
            "name": "PCI deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010961", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010961", 
            "name": "obesity and endocrinopathy due to impaired processing of Prohormones"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111698", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111698", 
            "name": "obesity and endocrinopathy due to impaired processing of prohormones"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111698", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111698", 
            "name": "PCI deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111698", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111698", 
            "name": "obesity due to prohormone convertase I deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111698", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111698", 
            "name": "obesity with impaired prohormone processing"
        }, 
        {
            "url": "https://www.omim.org/entry/600955", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:600955", 
            "name": "Proprotein convertase 1 deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111698", 
        "description": "A syndrome characterized by severe childhood obesity, hypoadrenalism,  hypogonadism, reactive hypoglycaemia, and elevated circulating levels of certain prohormones that has_material_basis_in homozygous or compound heterozygous mutation in PCSK1 on chromosome 5q15.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111698", 
        "name": "proprotein convertase 1/3 deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/600955", 
            "id": "600955", 
            "database": "MIM"
        }
    ]
}