{
    "disease_id": "DOID:14499", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Fd"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Anderson-Fabry disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "ceramide trihexosidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "deficiency of melibiase"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "diffuse angiokeratoma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Alpha-galactosidase A deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "hereditary dystopic lipidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "alpha galactosidase deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Fabry disease, Cardiac variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "angiokeratoma, diffuse"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "angiokeratoma corporis diffusum"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Gla deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010526", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010526", 
            "name": "Fabry's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14499", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14499", 
            "name": "Alpha-galactosidase A deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14499", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14499", 
            "name": "Angiokeratoma Corporis Diffusum"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14499", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14499", 
            "name": "Fabry's disease"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14499", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14499", 
            "name": "alpha galactosidase deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:14499", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:14499", 
            "name": "deficiency of melibiase"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:14499", 
        "description": "A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:14499", 
        "name": "Fabry disease"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/14499#disease-associations", 
            "id": "14499", 
            "database": "Alliance of Genome Resources"
        }
    ]
}