{
    "disease_id": "DOID:0090124", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "AMC neurogenic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "AMCN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "arthrogryposis multiplex congenita neurogenic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "neurogenic type of AMC"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "arthrogryposis multiplex congenita, neurogenic type; AMCN"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "AMC, neurogenic type"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0008823", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0008823", 
            "name": "arthrogryposis multiplex congenita, neurogenic type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090124", 
            "name": "AMC neurogenic type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090124", 
            "name": "AMCN"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090124", 
            "name": "arthrogryposis multiplex congenita neurogenic type"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090124", 
            "name": "AMC2"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0090124", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0090124", 
            "name": "arthrogryposis multiplex congenita 2, neurogenic type"
        }, 
        {
            "url": "https://www.omim.org/entry/208100", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:208100", 
            "name": "Arthrogryposis multiplex congenita, neurogenic type"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0090124", 
        "description": "A nervous system disease characterized by congenital contractures at the elbows and knees, myopathy, absence of muscle spindles, congenital heart disease and spinal motor neuron depletion, and has_material_basis_in autosomal recessive inheritance of homozygous mutation in the endoplasmic reticulum-golgi intermediate compartment protein 1 gene (ERGIC1) on chromosome region 5q35.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0090124", 
        "name": "neurogenic arthrogryposis multiplex congenita"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/208100", 
            "id": "208100", 
            "database": "MIM"
        }
    ]
}