{
    "disease_id": "DOID:0111540", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008221", 
            "name": "Peptidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008221", 
            "name": "hyperimidodipeptiduria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008221", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008221", 
            "name": "Imidodipeptidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111540", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111540", 
            "name": "hyperimidodipeptiduria"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111540", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111540", 
            "name": "imidodipeptidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111540", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111540", 
            "name": "peptidase deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111540", 
        "description": "An amino acid metabolic disorder characterized by massive imidodipeptiduria, chronic and slowly healing ulcerations, recurrent infections, dysmorphic facial features, variable cognitive impairment, splenomegaly, and lack of or reduced prolidase activity that has_material_basis_in homozygous or compound heterozygous mutation in PEPD on chromosome 19q13.11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111540", 
        "name": "prolidase deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111540#disease-associations", 
            "id": "0111540", 
            "database": "Alliance of Genome Resources"
        }
    ]
}