{
    "disease_id": "DOID:0050644",
    "recommended_name": {
        "id": "DOID:0050644",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0050644",
        "name": "arterial calcification of infancy",
        "description": "A vascular disease that is characterized by generalized calcification of the arterial internal elastic lamina, leading to rupture of the lamina and occlusive changes in the tunica intima with stenosis and decreased elasticity of the vessel wall."
    },
    "synonyms": [
        {
            "id": "DOID:0050644",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050644",
            "name": "generalized arterial calcification of infancy",
            "description": ""
        },
        {
            "id": "DOID:0050644",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050644",
            "name": "idiopathic infantile arterial calcification",
            "description": ""
        },
        {
            "id": "DOID:0050644",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0050644",
            "name": "infantile arteriosclerosis",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "arterial calcification, generalized, of infancy, 1",
            "description": "An autosomal recessive genetic disorder caused by mutations in the ENPP1 gene, encoding ectonucleotide pyrophosphatase/phosphodiesterase family member 1. The condition is characterized by calcification and narrowing of medium- and large-sized arteries, resulting in cardiovascular complications."
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "ENPP1 arterial calcification of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "arterial calcification of infancy caused by mutation in ENPP1",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "arterial calcification, generalized, of infancy, 1",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "arterial calcification, generalized, of infancy, type 1",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "generalised arterial calcification of infancy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "generalized arterial calcification of infancy 1",
            "description": ""
        },
        {
            "id": "MONDO:0008817",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0008817",
            "name": "GACI1",
            "description": ""
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "arterial calcification, generalized, of infancy, 2",
            "description": "Any arterial calcification of infancy in which the cause of the disease is a mutation in the ABCC6 gene."
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "ABCC6 arterial calcification of infancy",
            "description": ""
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "arterial calcification of infancy caused by mutation in ABCC6",
            "description": ""
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "arterial calcification, generalized, of infancy, 2",
            "description": ""
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "arterial calcification, generalized, of infancy, type 2",
            "description": ""
        },
        {
            "id": "MONDO:0013768",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013768",
            "name": "GACI2",
            "description": ""
        },
        {
            "id": "MIM:208000",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/208000",
            "name": "Arterial calcification of infancy, generalized, 1",
            "description": "Arterial calcification of infancy, generalized, 1"
        },
        {
            "id": "MIM:614473",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614473",
            "name": "Arterial calcification of infancy, generalized, 2",
            "description": "Arterial calcification of infancy, generalized, 2"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0050644"
    ],
    "unlinked_id_list": []
}