{
    "disease_id": "DOID:0061224",
    "recommended_name": {
        "id": "DOID:0061224",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0061224",
        "name": "Majeed syndrome",
        "description": "An autoinflammatory disease characterized by characterized by chronic recurrent multifocal osteomyelitis (CRMO) and congenital dyserythropoietic anemia that has_material_basis_in homozygous mutation in the LPIN2 gene on chromosome 18p11."
    },
    "synonyms": [
        {
            "id": "DOID:0061224",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0061224",
            "name": "chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "Majeed syndrome",
            "description": "Majeed syndrome is a rare genetic multisystemic disorder characterized by the triad of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and variable transient inflammatory dermatosis."
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "Majeed syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "CDA and CRMO",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "MJDS",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "chronic recurrent multifocal osteomyelitis, congenital",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "congenital dyserythropoietic anaemia and chronic recurrent multifocal osteomyelitis",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis",
            "description": ""
        },
        {
            "id": "MONDO:0012316",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0012316",
            "name": "dyserythropoietic anemia, and neutrophilic dermatosis",
            "description": ""
        },
        {
            "id": "MIM:609628",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/609628",
            "name": "Majeed syndrome",
            "description": "Majeed syndrome"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0061224"
    ],
    "unlinked_id_list": []
}