{
    "disease_id": "DOID:0110636",
    "recommended_name": {
        "id": "DOID:0110636",
        "resource": "Disease Ontology",
        "url": "https://disease-ontology.org/term/DOID:0110636",
        "name": "congenital merosin-deficient muscular dystrophy 1A",
        "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."
    },
    "synonyms": [
        {
            "id": "DOID:0110636",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110636",
            "name": "CMD1A",
            "description": ""
        },
        {
            "id": "DOID:0110636",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110636",
            "name": "MDC1A",
            "description": ""
        },
        {
            "id": "DOID:0110636",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110636",
            "name": "Merosin-negative congenital muscular dystrophy",
            "description": ""
        },
        {
            "id": "DOID:0110636",
            "resource": "Disease Ontology",
            "url": "https://disease-ontology.org/term/DOID:0110636",
            "name": "congenital muscular dystrophy due to laminin alpha2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "congenital merosin-deficient muscular dystrophy 1A",
            "description": "Congenital muscular dystrophy type 1A (MCD1A) belongs to a group of neuromuscular disorders with onset at birth or infancy characterized by hypotonia, muscle weakness and muscle wasting."
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "CMD1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "LAMA2 congenital muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "MDC1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "congenital merosin-deficient muscular dystrophy type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "congenital muscular dystrophy caused by mutation in LAMA2",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "congenital muscular dystrophy due to laminin alpha2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "merosin-deficient congenital muscular dystrophy type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "merosin-negative congenital muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "muscular dystrophy, congenital merosin-deficient, type 1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "muscular dystrophy, congenital, merosin deficient or partially deficient",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "LAMA2-related muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "laminin alpha-2 deficiency",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "merosin-deficient congenital muscular dystrophy",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "muscular dystrophy, congenital merosin-deficient, 1A",
            "description": ""
        },
        {
            "id": "MONDO:0011925",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0011925",
            "name": "muscular dystrophy, congenital, merosin-deficient",
            "description": ""
        },
        {
            "id": "MIM:607855",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/607855",
            "name": "Merosin-deficient congenital muscular dystrophy 1A",
            "description": "Merosin-deficient congenital muscular dystrophy 1A"
        }
    ],
    "children": [],
    "id_list": [
        "DOID:0110636"
    ],
    "unlinked_id_list": []
}