{
    "disease_id": "DOID:0090118", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011469", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011469", 
            "name": "CAMT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011469", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011469", 
            "name": "thrombocytopenia congenital amegakaryocytic"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011469", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011469", 
            "name": "amegakaryocytic thrombocytopenia, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011469", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011469", 
            "name": "amegakaryocytic thrombocytopenia, congenital; CAMT"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011469", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011469", 
            "name": "congenital amegakaryocytic thrombocytopenic purpura"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090118", 
            "name": "CAMT"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090118", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090118", 
            "name": "congenital amegakaryocytic thrombocytopenic purpura"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090118", 
        "description": "A thrombocytopenia that is characterized by a severe reduction in megakaryocyte and platelet numbers, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the myeloproliferative leukemia virus oncogene (MPL) on chromosome 1p34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090118", 
        "name": "congenital amegakaryocytic thrombocytopenia"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0090118#disease-associations", 
            "id": "0090118", 
            "database": "Alliance of Genome Resources"
        }
    ]
}