{
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "RHNR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "Rh-null disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "RH-null, regulator type; RHNR"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "Rh-null hemolytic Anemia, regulator type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "RH-null, regulator type; RHN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "Rh-null disease, regulator type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "RH-null, regulator type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "Rh-null syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "RHN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0019107", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0019107", 
            "name": "Rh-Mod"
        }, 
        {
            "url": "https://www.omim.org/entry/268150", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:268150", 
            "name": "Regulator type Rh-null hemolytic anemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050641", 
        "description": "A hemolytic anemia that is characterized by deficiency of Rh antigens, has_material_basis_in homozygous or compound heterozygous mutation in the RHAG gene on chromosome 6p12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050641", 
        "name": "Rh deficiency syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/268150", 
            "id": "268150", 
            "database": "MIM"
        }
    ]
}