{
    "disease_id": "DOID:0111583", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:0111583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111583", 
            "name": "anaphylotoxin inactivator deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111583", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111583", 
            "name": "deficiency of carboxypeptidase B"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111583", 
        "description": "A plasma protein metabolism disease characterized by low levels of carboxypeptidase N in the serum that may result in episodic angioedema, chronic urticaria, asthma and/or allergic hypersensitivity that has_material_basis_in homozygous or compound heterozygous mutation in CPN1 on chromosome 10q24.2.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111583", 
        "name": "carboxypeptidase N deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111583#disease-associations", 
            "id": "0111583", 
            "database": "Alliance of Genome Resources"
        }
    ]
}