{
    "disease_id": "DOID:0050638",
    "recommended_name": {
        "id": "DOID:0050638",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050638",
        "name": "hereditary systemic amyloidosis 1",
        "description": "An amyloidosis that is characterized by a loss of sensation in the extremities, cardiomyopathy, nephropathy, vitreous opacities, and CNS amyloidosis resulting from abnormal deposits of amyloid protein in the body's organs and tissues and has_material_basis_in autosomal dominant inheritance of mutations in the TTR gene."
    },
    "synonyms": [
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "Amyloidosis, hereditary, transthyretin-related",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "Corino de Andrade's disease",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "Familial transthyretin amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "TTR amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "familial amyloid polyneuropathy",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "transthyretin-related hereditary amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "ATTR amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "ATTRm amyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "paramyloidosis",
            "description": ""
        },
        {
            "id": "DOID:0050638",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050638",
            "name": "transthyretin amyloidosis",
            "description": ""
        },
        {
            "id": "MONDO:0971004",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0971004",
            "name": "amyloidosis, hereditary systemic 1",
            "description": ""
        },
        {
            "id": "MIM:105210",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/105210",
            "name": "Amyloidosis, hereditary systemic 1",
            "description": "Amyloidosis, hereditary systemic 1"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050638"
    ],
    "unlinked_id_list": []
}