{
    "disease_id": "DOID:0112107", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "McLeod neuroacanthocytosis syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "McLeod phenotype"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "X-linked McLeod syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "McLeod syndrome with chronic granulomatous disease"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "neuroacanthocytosis, McLeod type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "McLeod syndrome; MCLDS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "MLS"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0018945", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0018945", 
            "name": "MCLDS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112107", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112107", 
            "name": "McLeod neuroacanthocytosis syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112107", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112107", 
            "name": "MLS"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112107", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112107", 
            "name": "McLeod type neuroacanthocytosis"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112107", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112107", 
            "name": "X-linked McLeod syndrome"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112107", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112107", 
            "name": "McLeod syndrome with or without chronic granulomatous disease"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112107", 
        "description": "A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and  involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112107", 
        "name": "McLeod syndrome"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/300842", 
            "id": "300842", 
            "database": "MIM"
        }
    ]
}