{
    "disease_id": "DOID:0110636", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011925", 
            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        {
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            "description": "", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
            "name": "congenital muscular dystrophy due to laminin alpha2 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
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        }, 
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
            "name": "laminin alpha-2 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
            "name": "congenital muscular dystrophy caused by mutation in LAMA2"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
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        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
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            "name": "CMD1A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011925", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
            "name": "muscular dystrophy, congenital, due to partial LAMA2 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011925", 
            "name": "merosin-deficient congenital muscular dystrophy"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110636", 
            "name": "CMD1A"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110636", 
            "name": "MDC1A"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110636", 
            "name": "Merosin-negative congenital muscular dystrophy"
        }, 
        {
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            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110636", 
            "name": "congenital muscular dystrophy due to laminin alpha2 deficiency"
        }, 
        {
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            "description": "", 
            "resource": "MIM", 
            "id": "MIM:607855", 
            "name": "Merosin-deficient congenital muscular dystrophy 1A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110636", 
        "description": "A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscle weakness that is apparent at birth or in the first 6 months of life and frequent development of periventricular white matter abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the LAMA2 gene on chromosome 6q22.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110636", 
        "name": "congenital merosin-deficient muscular dystrophy 1A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/607855", 
            "id": "607855", 
            "database": "MIM"
        }
    ]
}