{
    "disease_id": "DOID:0070209", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "lymphedema, hereditary, 1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "lymphedema, hereditary, ID; LMPH1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "VEGFC hereditary lymphedema"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "lymphedema, hereditary, ID"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "hereditary lymphedema caused by mutation in VEGFC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "LMPH1D"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014393", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014393", 
            "name": "lymphedema, hereditary, type 1D"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070209", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070209", 
            "name": "LMPH1D"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070209", 
        "description": "A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the VEGFC gene on chromosome 4q34.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070209", 
        "name": "hereditary lymphedema ID"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070209#disease-associations", 
            "id": "0070209", 
            "database": "Alliance of Genome Resources"
        }
    ]
}