{
    "disease_id": "DOID:0050649", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "transferrin serum level quantitative trait locus 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "congenital atransferrinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "congenital hypotransferrinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "familial hypotransferrinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "hereditary atransferrinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008846", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008846", 
            "name": "hypotransferrinemia, familial"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050649", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050649", 
            "name": "familial hypotransferrinemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050649", 
        "description": "A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin on chromosome 3q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050649", 
        "name": "atransferrinemia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/209300", 
            "id": "209300", 
            "database": "MIM"
        }
    ]
}