{
    "disease_id": "DOID:0050990", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "episodic ataxia, type 2; EA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "CACNA1A hereditary episodic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "CAPA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "ataxia, familial, paroxysmal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "APCA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "EA2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "familial paroxysmal ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "cerebellar ataxia, paroxysmal, Acetazolamide-responsive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "ataxia, familial paroxysmal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "hereditary episodic ataxia caused by mutation in CACNA1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "ataxia, episodic, with Nystagmus"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "episodic ataxia, Nystagmus-associated"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "Acetazolamide-responsive episodic ataxia syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "Nystagmus-associated episodic ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "Cerebellopathy, hereditary paroxysmal"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "episodic ataxia, type 2"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0007163", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0007163", 
            "name": "episodic ataxia with nystagmus"
        }, 
        {
            "url": "https://www.omim.org/entry/108500", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:108500", 
            "name": "Episodic ataxia 2"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0050990", 
        "description": "An episodic ataxia that is characterized by periodic ataxia and nystagmus, and has_material_basis_in autosomal dominant inheritance of mutation in the calcium channel gene CACNA1A.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0050990", 
        "name": "episodic ataxia type 2"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/108500", 
            "id": "108500", 
            "database": "MIM"
        }
    ]
}