{
    "disease_id": "DOID:0060653", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "lethal congenital contracture syndrome 3; LCCS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "lethal congenital contracture syndrome caused by mutation in PIP5K1C"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "lethal congenital contracture syndrome type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "Israeli Bedouin type B multiple contracture syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "PIP5K1C lethal congenital contracture syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "LCCS3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0012656", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0012656", 
            "name": "multiple contracture syndrome, Israeli Bedouin type B"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0060653", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0060653", 
            "name": "Israeli Bedouin type B multiple contracture syndrome"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0060653", 
        "description": "A lethal congenital contracture syndrome that has_material_basis_in homozygous mutation in the PIP5K1C gene on chromosome 19p13.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0060653", 
        "name": "lethal congenital contracture syndrome 3"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/0060653#disease-associations", 
            "id": "0060653", 
            "database": "Alliance of Genome Resources"
        }
    ]
}