{
    "disease_id": "DOID:0070210",
    "recommended_name": {
        "id": "DOID:0070210",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0070210",
        "name": "hereditary lymphedema IA",
        "description": "A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the FLT4 gene on chromosome 5q35."
    },
    "synonyms": [
        {
            "id": "DOID:0070210",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0070210",
            "name": "LMPH1A",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "lymphedema, hereditary, 1A",
            "description": "Any hereditary lymphedema in which the cause of the disease is a mutation in the FLT4 gene."
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "lymphedema, hereditary, IA; LMPH1A",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "Milroy disease",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "FLT4 hereditary lymphedema",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "lymphedema, hereditary, IA",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "LMPH1A",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "lymphedema, early-onset",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "hereditary lymphedema caused by mutation in FLT4",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "primary congenital lymphedema",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "lymphedema, hereditary, type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0007919",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007919",
            "name": "Nonne-Milroy lymphedema",
            "description": ""
        },
        {
            "id": "MIM:153100",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/153100",
            "name": "Lymphatic malformation 1",
            "description": "Lymphatic malformation 1"
        }
    ]
}