{
    "disease_id": "DOID:0111509", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007922", 
            "name": "lymphedema with distichiasis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007922", 
            "name": "lymphedema-distichiasis syndrome with renal disease and diabetes mellitus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007922", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007922", 
            "name": "hereditary lymphedema-distichiasis syndrome (subtype)"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111509", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111509", 
            "name": "LPHDST"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111509", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111509", 
            "name": "lymphedema with distichiasis"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111509", 
        "description": "A syndrome characterized by lymphedema of the limbs and double rows of eyelashes that has_material_basis_in heterozygous mutation in FOXC2 on chromosome 16q24.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111509", 
        "name": "lymphedema-distichiasis syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111509#disease-associations", 
            "id": "0111509", 
            "database": "Alliance of Genome Resources"
        }
    ]
}