{
    "disease_id": "DOID:0112107",
    "recommended_name": {
        "id": "DOID:0112107",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0112107",
        "name": "McLeod syndrome",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0112107",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112107",
            "name": "MLS",
            "description": ""
        },
        {
            "id": "DOID:0112107",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112107",
            "name": "McLeod neuroacanthocytosis syndrome",
            "description": ""
        },
        {
            "id": "DOID:0112107",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112107",
            "name": "McLeod type neuroacanthocytosis",
            "description": ""
        },
        {
            "id": "DOID:0112107",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112107",
            "name": "X-linked McLeod syndrome",
            "description": ""
        },
        {
            "id": "DOID:0112107",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0112107",
            "name": "McLeod syndrome with or without chronic granulomatous disease",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "XK-related neurodegenerative disease",
            "description": "A form of neuroacanthocytosis and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens."
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "MLS",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "McLeod neuroacanthocytosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "McLeod syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "X-linked McLeod syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "XK disease",
            "description": ""
        },
        {
            "id": "MONDO:0018945",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0018945",
            "name": "MCLDS",
            "description": ""
        },
        {
            "id": "MIM:300842",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/300842",
            "name": "McLeod syndrome",
            "description": "McLeod syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112107"
    ],
    "unlinked_id_list": []
}