{
    "disease_id": "DOID:13382",
    "recommended_name": {
        "id": "DOID:13382",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13382",
        "name": "megaloblastic anemia",
        "description": "A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production."
    },
    "synonyms": [
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "Grasbeck-Imerslund syndrome",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "Imerslund-Grasbeck syndrome",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "MGA1 Norwegian type",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "RH-MGA1",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "megaloblastic anaemia",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "recessive hereditary megaloblastic anaemia 1",
            "description": ""
        },
        {
            "id": "DOID:13382",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13382",
            "name": "recessive hereditary megaloblastic anemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0013456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013456",
            "name": "constitutional megaloblastic anemia with severe neurologic disease",
            "description": ""
        },
        {
            "id": "MONDO:0013456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013456",
            "name": "megaloblastic anemia due to dihydrofolate reductase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013456",
            "name": "dihydrofolate reductase deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0013456",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013456",
            "name": "DHFR deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "Imerslund-Grasbeck syndrome",
            "description": "Imerslund-Grasbeck syndrome (IGS) or selective vitamin B12 (cobalamin) malabsorption with proteinuria is a rare autosomal recessive disorder characterized by vitamin B12 deficiency commonly resulting in megaloblastic anemia, which is responsive to parenteral vitamin B12 therapy and appears in childhood."
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "Grsbeck-Imerslund disease",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "Mga1",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "pernicious Anemia, juvenile, due to selective intestinal malabsorption of Vitamin B12, with Proteinuria",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "enterocyte cobalamin malabsorption",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "defect of enterocyte intrinsic factor receptor",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "selective cobalamin malabsorption with proteinuria",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "megaloblastic Anemia type 1",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "juvenile megaloblastic Anemia",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "enterocyte intrinsic Factor receptor, defect of",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "Imerslund-Grasbeck syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "Imerslund-Grsbeck syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "megaloblastic anemia 1",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "familial megaloblastic anemia",
            "description": ""
        },
        {
            "id": "MONDO:0009853",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009853",
            "name": "MGA-1",
            "description": ""
        },
        {
            "id": "MIM:613839",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613839",
            "name": "Megaloblastic anemia due to dihydrofolate reductase deficiency",
            "description": "Megaloblastic anemia due to dihydrofolate reductase deficiency"
        },
        {
            "id": "MIM:261100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/261100",
            "name": "Imerslund-Grasbeck syndrome 1",
            "description": "Imerslund-Grasbeck syndrome 1"
        }
    ]
}