{
    "disease_id": "DOID:13382", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "Imerslund-Grasbeck syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "Grsbeck-Imerslund disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "Mga1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "pernicious Anemia, juvenile, due to selective intestinal malabsorption of Vitamin B12, with Proteinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "enterocyte cobalamin malabsorption"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "defect of enterocyte intrinsic factor receptor"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "selective cobalamin malabsorption with proteinuria"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "megaloblastic Anemia type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "juvenile megaloblastic Anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "enterocyte intrinsic Factor receptor, defect of"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "Imerslund-Grsbeck syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "megaloblastic anemia 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "familial megaloblastic anemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009853", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009853", 
            "name": "MGA-1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "Grasbeck-Imerslund syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "Imerslund-Grasbeck syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "MGA1 Norwegian type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "RH-MGA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "megaloblastic anaemia"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "recessive hereditary megaloblastic anaemia 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:13382", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:13382", 
            "name": "recessive hereditary megaloblastic anemia 1"
        }, 
        {
            "url": "https://www.omim.org/entry/261100", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:261100", 
            "name": "Imerslund-Grasbeck syndrome 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:13382", 
        "description": "A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production.", 
        "resource": "Disease Ontology", 
        "id": "DOID:13382", 
        "name": "megaloblastic anemia"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/261100", 
            "id": "261100", 
            "database": "MIM"
        }
    ]
}