{
    "disease_id": "DOID:0080670", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "Meesmann corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "stocker-Holt dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "corneal dystrophy, Meesmann; MECD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "Meesmann corneal epithelial dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "corneal dystrophy, Meesmann"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "corneal dystrophy, juvenile epithelial of Meesmann"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "corneal dystrophy, juvenile epithelial, of Meesmann"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "Meesman dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "juvenile hereditary epithelial dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "juvenile hereditary epithelial dystrophy of Meesmann"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "corneal dystrophy, Meesmann epithelial"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "MECD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007379", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007379", 
            "name": "juvenile epithelial of Meesmann corneal dystrophy"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0080670", 
        "description": "A Messmann corneal dystrophy that is characterized by the presence of multitudinous microcysts within the anterior epithelium and that has_material_basis_in heterozygous mutation in the KRT12 gene on chromosome 17q21.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0080670", 
        "name": "Meesmann corneal dystrophy 1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0080670#disease-associations", 
            "id": "0080670", 
            "database": "Alliance of Genome Resources"
        }
    ]
}