{
    "disease_id": "DOID:13099",
    "recommended_name": {
        "id": "DOID:13099",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:13099",
        "name": "Moyamoya disease",
        "description": "A cerebral arterial disease characterized by constriction of certain arteries at the base of the brain. Blood flow is blocked by the constriction and also by blood clots."
    },
    "synonyms": [
        {
            "id": "DOID:13099",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:13099",
            "name": "progressive intracranial arterial occlusion",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "Moyamoya disease 5",
            "description": "Any Moyamoya disease in which the cause of the disease is a mutation in the ACTA2 gene."
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "Moyamoya disease caused by mutation in ACTA2",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "ACTA2 Moyamoya disease",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "MYMY5",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "Moyamoya disease type 5",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "Moyamoya disease 5",
            "description": ""
        },
        {
            "id": "MONDO:0013542",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013542",
            "name": "Moyamoya disease 5; MYMY5",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "MYMY1",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "Moyamoya disease",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "Moyamoya disease 1",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "MYMY1",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "spontaneous occlusion of the circle of Willis",
            "description": ""
        },
        {
            "id": "MONDO:0009649",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0009649",
            "name": "Moyamoya disease 1; MYMY1",
            "description": ""
        },
        {
            "id": "MONDO:0012122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012122",
            "name": "MYMY3",
            "description": ""
        },
        {
            "id": "MONDO:0012122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012122",
            "name": "Moyamoya disease 3; MYMY3",
            "description": ""
        },
        {
            "id": "MONDO:0012122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012122",
            "name": "Moyamoya disease 3",
            "description": ""
        },
        {
            "id": "MONDO:0012122",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012122",
            "name": "MYMY3",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome",
            "description": "Moyamoya angiopathy - short stature - facial dysmorphism - hypergonadotropic hypogonadism is a very rare, hereditary, neurological, dysmorphic syndrome characterized by moyamoya disease, short stature of postnatal onset, and stereotyped facial dysmorphism."
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "MYMY4",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "syndromic Moyamoya disease",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism; MYMY4",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "Moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism",
            "description": ""
        },
        {
            "id": "MONDO:0010448",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010448",
            "name": "chromosome Xq28 deletion syndrome, 3.4-Kb",
            "description": ""
        },
        {
            "id": "MONDO:0014331",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014331",
            "name": "Moyamoya disease with early-onset achalasia",
            "description": "Moyamoya disease with early-onset achalasia is an exceedingly rare autosomal recessive neurological disorder reported only in a few families so far. It is characterized by the association of early onset achalasia (manifesting in infancy) with severe intracranial angiopathy that is consistent with moyamoya angiopathy in most cases (moyamoya disease; see this term). Other variable associated manifestations include hypertension, Raynaud phenomenon, and livedo reticularis."
        },
        {
            "id": "MONDO:0014331",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014331",
            "name": "MYMY6",
            "description": ""
        },
        {
            "id": "MONDO:0014331",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014331",
            "name": "Moyamoya disease 6 with achalasia",
            "description": ""
        },
        {
            "id": "MONDO:0014331",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0014331",
            "name": "Moyamoya disease 6 with achalasia; MYMY6",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "Moyamoya disease 2",
            "description": "Any Moyamoya disease in which the cause of the disease is a mutation in the RNF213 gene."
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "Moyamoya disease caused by mutation in RNF213",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "MYMY2",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "Moyamoya disease type 2",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "Moyamoya disease 2; MYMY2",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "Moyamoya disease 2",
            "description": ""
        },
        {
            "id": "MONDO:0011784",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011784",
            "name": "RNF213 Moyamoya disease",
            "description": ""
        },
        {
            "id": "MIM:614042",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/614042",
            "name": "Moyamoya disease 5",
            "description": "Moyamoya disease 5"
        },
        {
            "id": "MIM:615750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/615750",
            "name": "Moyamoya disease 6 with or without achalasia",
            "description": "Moyamoya disease 6 with or without achalasia"
        },
        {
            "id": "MIM:607151",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607151",
            "name": "Moyamoya disease 2",
            "description": "Moyamoya disease 2"
        }
    ]
}