{
    "disease_id": "DOID:0060866", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "macular dystrophy, patterned, 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "patterned dystrophy of retinal pigment epithelium"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "butterfly-shaped pigmentary maculary dystrophy 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "macular dystrophy, patterned, type 1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "PRPH2 patterned macular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "butterfly-shaped pigment dystrophy of the fovea"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "macular dystrophy, patterned, 1; MDPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "MDPT1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "patterned macular dystrophy caused by mutation in PRPH2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "macular dystrophy, butterfly-Shaped pigmentary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "butterfly dystrophy of retinal pigment epithelium"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008210", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008210", 
            "name": "patterned macular dystrophy type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060866", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060866", 
            "name": "MDPT1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060866", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060866", 
            "name": "butterfly-shaped pigmentary maculary dystrophy 1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060866", 
        "description": "A patterned macular dystrophy characterized by bilateral accumulation of pigmented or yellowish material at the level of the retinal pigment epithelium in lesions that resemble the wings of a butterfly that has material_basis_in heterozygous mutation in the PRPH2 gene on chromosome 6p21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060866", 
        "name": "patterned macular dystrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060866#disease-associations", 
            "id": "0060866", 
            "database": "Alliance of Genome Resources"
        }
    ]
}