{
    "disease_id": "DOID:0110635", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5; MDDGB5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "MDC1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "FKRP-related congenital muscular dystrophy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "muscular dystrophy, congenital, 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "muscular dystrophy, congenital, FKRP-related"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "congenital muscular dystrophy 1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011688", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011688", 
            "name": "MDDGB5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "FKRP-related congenital muscular dystrophy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "MDC1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "MDDGB5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "congenital muscular dystrophy 1C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110635", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110635", 
            "name": "muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110635", 
        "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110635", 
        "name": "muscular dystrophy-dystroglycanopathy type B5"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110635#disease-associations", 
            "id": "0110635", 
            "database": "Alliance of Genome Resources"
        }
    ]
}