{
    "disease_id": "DOID:0090028", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "VITAMIN E, familial isolated deficiency OF"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "Friedreich-like ataxia with selective vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "Friedreich-like ataxia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "familial isolated vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "VITAMIN E, familial isolated deficiency OF; VED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "isolated vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "ataxia with vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "VED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "ataxia, Friedreich-like, with selective Vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "AVED"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "ataxia with isolated vitamin E deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010188", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010188", 
            "name": "familial isolated deficiency of vitamin type E"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090028", 
            "name": "ataxia with isolated vitamin E deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090028", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090028", 
            "name": "familial isolated vitamin E deficiency"
        }, 
        {
            "url": "https://www.omim.org/entry/277460", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:277460", 
            "name": "Ataxia with isolated vitamin E deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090028", 
        "description": "A vitamin metabolic disorder characterized by progressive spino-cerebellar ataxia, loss of proprioception, areflexia, and marked deficiency in vitamin E that has_material_basis_in homozygous or compound heterozygous mutation in the TTPA gene on chromosome 8q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090028", 
        "name": "familial isolated deficiency of vitamin E"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/277460", 
            "id": "277460", 
            "database": "MIM"
        }
    ]
}