{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "PFD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "complement Factor properdin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin P Factor deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "CFPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency, X-linked; CFPD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010713", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010713", 
            "name": "properdin deficiency, X-linked"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111768", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111768", 
            "name": "CFPD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111768", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111768", 
            "name": "complement factor properdin deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/312060", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:312060", 
            "name": "Properdin deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111768", 
        "description": "A complement deficiency characterized by decreased plasma levels of complement factor properdin and increased susceptibility to Neisseria species infections that has_material_basis_in homozygous or hemizygous mutation in PFC on chromosome Xp11.23.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111768", 
        "name": "X-linked properdin deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/312060", 
            "id": "312060", 
            "database": "MIM"
        }
    ]
}