{
    "disease_id": "DOID:0050637", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloidosis V"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "meretoja type amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "lattice corneal dystrophy type II Finnish"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "cerebral amyloid angiopathy, Gsn-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "hereditary amyloidosis, Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloidosis, Meretoja type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "corneal dystrophy, lattice type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "hereditary gelsolin amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "AGel amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloidosis 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "gelsolin amyloidosis"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloid cranial neuropathy with lattice corneal dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "familial amyloid polyneuropathy type IV"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloidosis, Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "lattice corneal dystrophy, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "amyloidosis due to mutant gelsolin"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "familial amyloidosis, Finnish type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007097", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007097", 
            "name": "meretoja syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0050637", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0050637", 
            "name": "AMYLOIDOSIS, MERETOJA TYPE"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050637", 
        "description": "An amyloidosis that is characterized by abnormal deposits of amyloid protein that mainly affect the eyes, nerves and skin and has_material_basis_in mutations in the gelsolin gene (GSN), and has_symptoms corneal lattice dystrophy, has_symptom bilateral facial paralysis, has_symptom cutis laxa.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050637", 
        "name": "Finnish type amyloidosis"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0050637#disease-associations", 
            "id": "0050637", 
            "database": "Alliance of Genome Resources"
        }
    ]
}