{
    "disease_id": "DOID:0060456", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "corneal dystrophy crystalline of Schnyder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "Schnyder crystalline dystrophy sine crystals"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "corneal dystrophy, crystalline, of Schnyder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "SCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "SCCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "crystalline stromal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "hereditary crystalline stromal dystrophy of Schnyder"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "Schnyder crystalline corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "Schnyder corneal dystrophy; SCCD"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007374", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007374", 
            "name": "corneal dystrophy, Schnyder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060456", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060456", 
            "name": "SCCD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060456", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060456", 
            "name": "Schnyder crystalline corneal dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060456", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060456", 
            "name": "corneal dystrophy crystalline of Schnyder"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060456", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060456", 
            "name": "crystalline stromal dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060456", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060456", 
            "name": "hereditary crystalline stromal dystrophy of Schnyder"
        }, 
        {
            "url": "https://www.omim.org/entry/121800", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:121800", 
            "name": "Corneal dystrophy, Schnyder type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060456", 
        "description": "A stromal dystrophy that is characterized by abnormal deposition of cholesterol and phospholipids in the cornea and that has_material_basis_in heterozygous mutation in the UBAID1 gene on chromosome 1p36.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060456", 
        "name": "Schnyder corneal dystrophy"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/121800", 
            "id": "121800", 
            "database": "MIM"
        }
    ]
}