{
    "disease_id": "DOID:0112378",
    "recommended_name": {
        "id": "DOID:0112378",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:0112378",
        "name": "muscular dystrophy-dystroglycanopathy type B3",
        "description": "A muscular dystrophy-dystroglycanopathy type B that has_material_basis_in homozygous or compound heterozygous mutation in the POMGNT1 gene on chromosome 1p34.1."
    },
    "synonyms": [
        {
            "id": "DOID:0112378",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112378",
            "name": "MDDGB3",
            "description": ""
        },
        {
            "id": "DOID:0112378",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:0112378",
            "name": "congenital muscular dystrophy POMGNT1-related",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "congenital muscular dystrophy-POMGNT1 related",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "MDDGB3",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "muscular dystrophy, congenital, POMGNT1-related",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 3",
            "description": ""
        },
        {
            "id": "MONDO:0013155",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013155",
            "name": "muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3",
            "description": ""
        },
        {
            "id": "MIM:613151",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613151",
            "name": "Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B3",
            "description": "Muscular dystrophy-dystroglycanopathy congenital with impaired intellectual development B3"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0112378"
    ],
    "unlinked_id_list": []
}