{
    "disease_id": "DOID:13636", 
    "synonyms": [
        {
            "url": "http://disease-ontology.org/term/DOID:13636", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13636", 
            "name": "Fanconi panmyelopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13636", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13636", 
            "name": "Fanconi's anemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13636", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13636", 
            "name": "Fanconi's anaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13636", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13636", 
            "name": "Fanconi pancytopenia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13636", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13636", 
            "name": "Fanconi anaemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "Fanconi anemia caused by mutations of the FANCA gene. FANCA gene mutations are the most common cause of Fanconi anemia. This gene provides instructions for making a protein that is involved in the Fanconi anemia (FA) pathway.", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi anemia complementation group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi Anemia, Estren-Dameshek variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Estren-Dameshek variant of Fanconi pancytopenia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi anemia caused by mutation in FANCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "FANCA Fanconi anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi anemia, complementation group A; FANCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Estren-Dameshek variant of Fanconi Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "FANCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi Anemia, complementation group type a"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi anemia, complementation group A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009215", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009215", 
            "name": "Fanconi anemia complementation group type A"
        }, 
        {
            "url": "https://www.omim.org/entry/227650", 
            "description": "Fanconi anemia, complementation group A", 
            "resource": "MIM", 
            "id": "MIM:227650", 
            "name": "Fanconi anemia, complementation group A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13636", 
        "description": "A congenital hypoplastic anemia characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors. It is a result of a genetic defect in a cluster of proteins responsible for DNA repair.", 
        "resource": "Disease Ontology", 
        "id": "DOID:13636", 
        "name": "Fanconi anemia"
    }
}