{
    "disease_id": "DOID:0050734",
    "recommended_name": {
        "id": "DOID:0050734",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0050734",
        "name": "congenital intrinsic factor deficiency",
        "description": "A vitamin B12 deficiency that is characterized by megaloblastic anemia due to the absence of gastric intrinsic factor which results in abnormal vitamin B12 absorption."
    },
    "synonyms": [
        {
            "id": "DOID:0050734",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0050734",
            "name": "hereditary intrinsic factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "congenital intrinsic factor deficiency",
            "description": "Congenital intrinsic factor deficiency (IFD) is a rare disorder of vitamin B12 (cobalamin) absorption that is characterized by megaloblastic anemia and neurological abnormalities."
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "intrinsic factor, congenital deficiency of",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "IFD",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "intrinsic factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "congenital pernicious anemia due to defect of intrinsic factor",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "congenital pernicious anemia",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "pernicious Anemia, congenital, due to defect of intrinsic Factor",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "intrinsic factor deficiency; IFD",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "gastric intrinsic factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "hereditary intrinsic factor deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009852",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009852",
            "name": "hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency",
            "description": ""
        },
        {
            "id": "MIM:261000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/261000",
            "name": "Hereditary intrinsic factor deficiency",
            "description": "Hereditary intrinsic factor deficiency"
        }
    ]
}