{
    "disease_id": "DOID:0111600", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "Sheldon-hall syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "Freeman Sheldon variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis multiplex congenita, distal, type II, with craniofacial abnormalities"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis, distal, type 2B; DA2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "Freeman-Sheldon syndrome variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis multiplex congenita, distal, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis multiplex congenita distal type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "Freeman Sheldon syndrome, variant"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "DA2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis, distal, type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "distal arthrogryposis type 2B"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0011128", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0011128", 
            "name": "arthrogryposis multiplex congenita distal type II with craniofacial abnormalities"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0111600", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0111600", 
            "name": "DA2B1"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0111600", 
        "description": "A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in TNNI2 on chromosome 11p15.5.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0111600", 
        "name": "distal arthrogryposis type 2B1"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0111600#disease-associations", 
            "id": "0111600", 
            "database": "Alliance of Genome Resources"
        }
    ]
}