{
    "disease_id": "DOID:0070208", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "lymphedema, hereditary, 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "lymphedema, hereditary, IC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "GJC2 hereditary lymphedema"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "LMPH1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "lymphedema, hereditary, type 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "hereditary lymphedema caused by mutation in GJC2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013278", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013278", 
            "name": "lymphedema, hereditary, IC; LMPH1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0070208", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0070208", 
            "name": "LMPH1C"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0070208", 
        "description": "A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the GJC2 gene on chromosome 1q42.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0070208", 
        "name": "hereditary lymphedema IC"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0070208#disease-associations", 
            "id": "0070208", 
            "database": "Alliance of Genome Resources"
        }
    ]
}