{
    "disease_id": "DOID:0060865", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "MAPKAPK3 patterned macular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "MCRPE"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "patterned macular dystrophy type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "macular dystrophy, patterned, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "Martinique crinkled retinal pigment epitheliopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "MDPT3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "macular dystrophy, patterned, 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "patterned macular dystrophy caused by mutation in MAPKAPK3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0014920", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0014920", 
            "name": "macular dystrophy, patterned, 3; MDPT3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060865", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060865", 
            "name": "MDPT3"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060865", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060865", 
            "name": "Martinique crinkled retinal pigment epitheliopathy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060865", 
        "description": "A patterned macular dystrophy characterized by a 'dry desert land' pattern of the fundus, involving the posterior pole initially and progressing from the temporal fovea to the periphery of the retina developing in the fourth or fifth decade of life that has material_basis_in heterozygous mutation in the MAPKAPK3 gene on chromosome 3p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060865", 
        "name": "patterned macular dystrophy 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060865#disease-associations", 
            "id": "0060865", 
            "database": "Alliance of Genome Resources"
        }
    ]
}