{
    "disease_id": "DOID:0050637",
    "recommended_name": {
        "id": "DOID:0050637",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050637",
        "name": "Finnish type amyloidosis",
        "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_symptom corneal lattice dystrophy, has_symptom bilateral facial paralysis, has_symptom cutis laxa."
    },
    "synonyms": [
        {
            "id": "DOID:0050637",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050637",
            "name": "AMYLOIDOSIS, MERETOJA TYPE",
            "description": ""
        },
        {
            "id": "DOID:0050637",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050637",
            "name": "AGel amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050637",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050637",
            "name": "Lattice corneal dystrophy type II",
            "description": ""
        },
        {
            "id": "DOID:0050637",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050637",
            "name": "gelsolin amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "Finnish type amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "amyloidosis, MERETOJA type",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "familial amyloid polyneuropathy type IV",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "familial amyloidosis, Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "gelsolin amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "hereditary amyloidosis, Finnish type",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "meretoja syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "amyloidosis V",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "hereditary gelsolin amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0007097",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0007097",
            "name": "lattice corneal dystrophy type II Finnish",
            "description": ""
        },
        {
            "id": "MIM:105120",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/105120",
            "name": "Amyloidosis, hereditary systemic 4, Finnish type",
            "description": "Amyloidosis, hereditary systemic 4, Finnish type"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050637"
    ],
    "unlinked_id_list": []
}