{
    "disease_id": "DOID:0110277", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
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            "name": "sarcoglycan, gamma, deficiency of"
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            "description": "", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "muscular dystrophy, Duchenne-like"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "Adhalin deficiency, secondary"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "SGCG autosomal recessive limb-girdle muscular dystrophy"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "Maghrebian myopathy"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "severe childhood autosomal recessive muscular dystrophy, North African type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "deficiency of sarcoglycan gamma"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
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        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "muscular dystrophy, limb-girdle, type 2C; LGMD2C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0009677", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0009677", 
            "name": "severe childhood autosomal recessive muscular dystrophy North African type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "autosomal recessive Duchenne-like muscular dystrophy type 1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "severe childhood autosomal recessive muscular dystrophy North African type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "DMDA1"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "LGMD2C"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "Maghrebian myopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "SCARMD"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "deficiency of sarcoglycan gamma"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "gamma-sarcoglycanopathy"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
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        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110277", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110277", 
            "name": "limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110277", 
        "description": "An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gamma-sarcoglycan gene (SGCG) on chromosome 13q12.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110277", 
        "name": "autosomal recessive limb-girdle muscular dystrophy type 2C"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0110277#disease-associations", 
            "id": "0110277", 
            "database": "Alliance of Genome Resources"
        }
    ]
}