{
    "disease_id": "DOID:0112001", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "combined immunodeficiency due to moesin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "IMD50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "immunodeficiency type 50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "MSN-related combined immunodeficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "immunodeficiency 50, X-linked recessive"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "Cid due to Moesin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "immunodeficiency 50; IMD50"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010514", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010514", 
            "name": "X-linked Moesin-associated immunodeficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "IMD50"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "CID due to Moesin deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "MSN-related combined immunodeficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "X-linked Moesin-associated immunodeficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "combined immunodeficiency due to Moesin deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0112001", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0112001", 
            "name": "immunodeficiency 50 X linked recessive"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0112001", 
        "description": "A combined immunodeficiency characterized by profound lymphopenia, hypogammaglobulinemia, poor immune response to vaccine antigens, fluctuating neutropenia and onset in early childhood of recurrent bacterial or varicella zoster virus infections that has_material_basis_in hemizygous mutation in MSN on chromosome Xq12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0112001", 
        "name": "immunodeficiency 50"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0112001#disease-associations", 
            "id": "0112001", 
            "database": "Alliance of Genome Resources"
        }
    ]
}